Bangalore Healthcare Jobs

Why This Role MattersPharmacovigilance is essential for ensuring the safety and effectiveness of medicines throughout their lifecycle. From clinical trials to post-marketing surveillance, pharmacovigilance professionals monitor adverse events, analyze safety data, and ensure that pharmaceutical products comply with global regulatory requirements. The Pharmacovigilance Associate role at Alvotech plays a key part in supporting global safety data management for biosimilar medicines. The position contributes to the monitoring of safety data generated from clinical trials and post-marketing programs while maintaining compliance with international pharmacovigilance regulations.Working within the Global Safety Data Management team, the PV Associate will assist in managing adverse event reports, monitoring safety signals, and supporting pharmacovigilance system operations. This role also contributes to improving pharmacovigilance processes and ensuring regulatory compliance across global safety programs. For professionals with pharmacovigilance experience, this role offers valuable exposure to global drug safety operations, safety databases, and regulatory frameworks governing biosimilar medicines.Job DescriptionAlvotech is seeking a motivated Pharmacovigilance Associate to support clinical safety and post-marketing pharmacovigilance activities within its Research and Development function. The selected candidate will be part of the Global Safety Data Management team and will contribute to safety data handling, regulatory reporting, and pharmacovigilance process development. The role involves working with safety databases, managing adverse event cases, and ensuring that safety information is processed in accordance with international regulatory requirements.The PV Associate will collaborate with multiple internal departments and external partners to ensure timely safety reporting and regulatory compliance across global clinical and post-marketing programs.Key Features of the Role• Opportunity to work within global pharmacovigilance and safety data management• Exposure to clinical trial safety monitoring and post-marketing surveillance• Involvement in pharmacovigilance system configuration and lifecycle management• Collaboration with global regulatory, quality, and clinical teams• Participation in safety process improvement and compliance initiatives• Opportunity to support safety monitoring for biosimilar medicinesResponsibilitiesClinical Safety & Pharmacovigilance Activities• Support assigned clinical safety and post-marketing pharmacovigilance activities• Manage Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) processing• Assist in regulatory safety submissions and reporting requirements• Perform literature monitoring and digital platform monitoring for safety signals• Conduct pharmacovigilance reconciliations and safety data verification• Support activities related to EudraVigilance and XEVMPDSafety Systems & Data Management• Assist in configuration, validation, and lifecycle management of pharmacovigilance systems• Maintain safety databases and ensure accurate safety data management• Work with safety systems such as Oracle Argus Safety, ARISg Safety System, and Veeva Vault SafetyPharmacovigilance Process Support• Assist in maintaining and optimizing global pharmacovigilance procedures• Ensure compliance with internal SOPs and international safety regulations• Support safety documentation and regulatory compliance activitiesCross-Functional Collaboration• Work with pharmacovigilance teams involved in benefit-risk management and clinical trials• Collaborate with departments such as Quality, Regulatory Affairs, IT, and Clinical Program Development• Coordinate with external pharmacovigilance service providers and business partnersTraining, Audits & Compliance• Support pharmacovigilance training for internal staff and external stakeholders• Assist in safety-related audits and regulatory inspections• Maintain accurate documentation to meet global regulatory requirementsRequired QualificationsEducational Requirements• Master’s degree in Pharmaceutical Sciences, Pharmacy, Medicine, or Life SciencesExperience and Skills• Minimum 2 years of experience in Pharmacovigilance or Drug Safety• Experience working in safety data management functions• Hands-on experience in clinical trial safety and post-marketing pharmacovigilance• Familiarity with pharmacovigilance safety databases• Experience working with global pharmaceutical products and clinical trials• Knowledge of biologic or combination products is considered an advantageRegulatory Knowledge• Understanding of global pharmacovigilance regulations including• ICH Guidelines• FDA Regulations• Good Pharmacovigilance Practices• Good Clinical Practice• Council for International Organizations of Medical Sciences safety reporting standardsProfessional Skills• Strong organizational and time-management skills• Excellent written and verbal communication abilities• Ability to manage multiple safety activities and meet deadlines• Capability to work independently and collaboratively in multicultural teamsSalary InsightsAlthough the exact salary has not been specified, Pharmacovigilance Associate roles in the global biopharmaceutical industry typically offer competitive compensation based on experience, location, and expertise. Employees may also receive additional benefits such as professional development opportunities, global project exposure, and involvement in innovative biosimilar research programs.Company OverviewAlvotech is a global biopharmaceutical company focused on developing and manufacturing high-quality biosimilar medicines.The company specializes in improving access to biologic treatments by producing cost-effective biosimilars while maintaining strict regulatory, safety, and quality standards. Within its Research and Development division, the Integrated Clinical and Medical Research department develops strategies aligned with global biosimilar guidelines and regulatory authority requirements to support successful clinical studies and post-marketing safety programs.Through advanced pharmacovigilance systems and global safety monitoring processes, Alvotech ensures that its biosimilar medicines meet international safety and regulatory standards.FAQsWho can apply for this role?Candidates with a Master’s degree in Pharmacy, Life Sciences, or Medicine and at least 2 years of pharmacovigilance experience.What type of work does the PV Associate perform?The role involves adverse event case processing, safety monitoring, regulatory reporting, safety database management, and pharmacovigilance compliance activities.Is experience with safety databases required?Yes. Experience with systems such as Argus, ARISg, or Veeva Vault Safety is preferred.Does the role involve working with clinical trials?Yes. The position supports safety monitoring for both clinical trials and post-marketing pharmacovigilance programs.Application Tips• Highlight your pharmacovigilance experience and safety data management expertise• Include experience working with ICSR processing and SAE reporting• Mention knowledge of safety databases such as Argus or Veeva Vault Safety• Demonstrate familiarity with global PV regulations such as ICH, GVP, and GCP guidelines• Emphasize strong documentation practices and attention to detail

Why This Role MattersThe Senior Associate – Data Sciences in Global Market Vigilance plays a key role in monitoring product safety and post-market surveillance data across global markets. The position focuses on safety analytics, signal detection, and regulatory compliance to ensure that adverse event trends are identified early and managed effectively, supporting consumer safety and regulatory requirements.Job DescriptionUnilever is hiring a Senior Associate – Data Sciences within the Global Market Vigilance (GMV) team at its R&D center in Bengaluru. The role focuses on pharmacovigilance data analytics, adverse event case management, and signal detection activities while ensuring compliance with global regulatory standards and maintaining inspection readiness.Key Features of the Role• Opportunity to work in global pharmacovigilance and safety data analytics• Exposure to post-market surveillance and safety monitoring processes• Hands-on work with safety databases and advanced analytics tools• Collaboration with regulatory affairs, R&D, and quality teams• Involvement in global adverse event trending and signal detection activitiesResponsibilitiesCase Management and Compliance• Lead or perform adverse event intake, triage, and documentation using safety systems such as Veeva Vault Safety• Conduct duplicate checks and ensure high-quality safety data for analysis• Perform seriousness, causality, and expectedness assessments with proper documentation• Ensure compliance with MedDRA coding standards, SOPs, and global adverse event reporting requirementsSafety Data Analytics, Trending and Signal Detection• Perform quantitative and qualitative safety data analysis across brands and markets• Develop dashboards, KPIs, and safety scorecards for monitoring trends• Conduct global adverse event trending, signal detection, and safety pattern analysis• Validate potential safety signals through case series evaluation and confounder assessments• Support automation initiatives across the pharmacovigilance lifecycleSystem and Process Optimization• Support configuration, testing, and validation of pharmacovigilance safety databases• Perform safety data audits, reconciliation, and root cause investigations• Implement process improvements to enhance data integrity and analytics readinessCross-Functional Collaboration and Leadership• Act as the analytics and safety contact for regulatory affairs, R&D, quality teams, and customer support groups• Present safety trends, risks, and signals to stakeholders and governance forums• Mentor junior associates in pharmacovigilance analytics and documentation standards• Drive corrective and preventive actions related to safety data issuesRequired QualificationsEducational Requirements• Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or a related fieldExperience and Skills• 5–8 years of experience in pharmacovigilance, safety analytics, or global market vigilance• Hands-on experience with pharmacovigilance systems such as Veeva Vault Safety or similar platforms• Strong knowledge of safety data trending, signal detection, and pharmacovigilance analytics• Experience with analytics tools such as Power BI, Tableau, SQL, or advanced Excel• Familiarity with automation or AI-enabled pharmacovigilance workflows• Strong understanding of audit readiness, quality management systems, and vendor oversight]Salary InsightsSalary details were not specified in the job posting and are expected to be offered as per company standards and experience.Company OverviewUnilever is a global consumer goods company known for its wide portfolio of health, beauty, and wellbeing products. The company invests heavily in research and development to ensure product safety, quality, and regulatory compliance across international markets.FAQs• What qualification is required for this role?Candidates should have a bachelor’s or master’s degree in life sciences, pharmacy, or a related discipline.• How much experience is required?Applicants should have approximately 5–8 years of experience in pharmacovigilance, safety analytics, or post-market surveillance.• Where is the job located?The role is based at the Unilever R&D center in Bengaluru, Karnataka.• What type of work will the candidate perform?The role involves pharmacovigilance data analytics, adverse event case management, signal detection, and safety trend monitoring.Application Tips• Highlight experience in pharmacovigilance systems and safety data analysis• Mention knowledge of MedDRA coding and adverse event processing• Include experience with analytics tools such as Power BI, Tableau, or SQL• Showcase expertise in signal detection and pharmacovigilance compliance• Demonstrate strong documentation and regulatory compliance skills

Why This Role MattersClinical trials generate large volumes of complex data that must be accurately collected, managed, and analyzed to support regulatory submissions and scientific decision-making. Clinical Data Management plays a critical role in ensuring that this data is reliable, consistent, and compliant with regulatory standards. The Associate Manager – Clinical Data Management supports the successful execution of clinical research projects by overseeing data management activities throughout the clinical trial lifecycle. This includes designing data collection systems, managing clinical databases, and ensuring that clinical trial data meets strict quality and regulatory requirements. In modern clinical research, data quality is essential for maintaining the integrity of study results and ensuring patient safety. Data management professionals ensure that clinical data is accurate, complete, and ready for statistical analysis and regulatory review.Another important aspect of the role involves collaboration with cross-functional teams such as clinical operations, biostatistics, and external vendors. By coordinating data management activities across these groups, the Associate Manager helps ensure that clinical trial milestones are achieved efficiently. The role also involves implementing data standards, maintaining documentation, and supporting regulatory inspections or audits. Strong oversight of external vendors and contract research organizations is essential to ensure that all deliverables meet quality expectations and project timelines. For professionals experienced in clinical data management, this position provides an opportunity to lead data-related activities within global clinical trials while contributing to the development of high-quality healthcare products. Overall, the role supports the successful management of clinical trial data, enabling pharmaceutical and healthcare companies to generate reliable evidence for regulatory approvals and product development.Job DescriptionThe Associate Manager – Clinical Data Management is responsible for planning, coordinating, and overseeing data management activities related to clinical research projects. The role ensures that clinical trial data is collected, processed, and maintained in compliance with regulatory guidelines and organizational standards. Professionals in this role manage the design and implementation of data management tasks for clinical studies, including the development of electronic data capture systems and data management plans. They collaborate closely with clinical and biostatistics teams to ensure that study data meets the requirements for statistical analysis and regulatory submissions. The position also involves managing data collection systems such as Electronic Data Capture (EDC) platforms and integrating data from external systems including electronic patient-reported outcomes and other clinical data sources. In addition to technical responsibilities, the Associate Manager provides oversight of external vendors responsible for data management services. This includes evaluating vendor proposals, monitoring service delivery, and ensuring compliance with service-level agreements. The role also includes reviewing study documentation, organizing data quality review meetings, and ensuring that clinical datasets remain accurate and complete throughout the study lifecycle. Overall, the position combines leadership, data management expertise, and cross-functional collaboration to ensure the successful delivery of high-quality clinical trial data.Key Features of the Role:• Leadership role within clinical data management operations.• Opportunity to manage end-to-end clinical trial data processes.• Collaboration with clinical operations, biostatistics, and regulatory teams.• Involvement in data quality management and regulatory compliance.• Exposure to advanced clinical data systems and digital data collection tools.• Opportunity to oversee external vendors and CRO partners.• Participation in global clinical research projects.• Career development in clinical data management and clinical research leadership.Responsibilities• Plan and manage data management activities for clinical research projects.• Design and implement data management solutions for complex clinical studies.• Ensure all data management activities comply with regulatory guidelines and quality standards.• Coordinate with clinical and biostatistics teams to support clinical data analysis.• Manage electronic data capture systems and other clinical data collection platforms.• Author and review data management study documents including Data Management Plans and eCRF guidelines.• Conduct data quality review meetings with cross-functional study teams.• Monitor and ensure data accuracy, completeness, and consistency throughout clinical trials.• Provide oversight to external vendors and contract research organizations responsible for data management deliverables.• Evaluate proposals from external service providers and manage vendor relationships.• Maintain clinical data standards and support the development of standardized data structures.• Support regulatory inspections and audits related to clinical data management.• Mentor junior team members and support their professional development.Required Qualifications• Strong understanding of clinical data management processes.• Knowledge of clinical trial regulations and industry standards.• Ability to manage complex projects and coordinate cross-functional teams.• Strong analytical and problem-solving skills.• Excellent communication and stakeholder management abilities.Educational Requirements• Bachelor’s degree in Mathematics, Science, Pharmacy, Life Sciences, or a related field.Experience and Skills• Minimum of 8 years of clinical data management experience in the healthcare or pharmaceutical industry.• Strong knowledge of clinical trial regulations including International Council for Harmonisation guidelines and Good Clinical Practice standards.• Experience working with Clinical Data Management Systems (CDMS) and Electronic Data Capture platforms.• Experience integrating data from multiple clinical data sources such as eCOA and external datasets.• Strong project management and organizational skills.• Experience managing vendor relationships and service delivery agreements.• Ability to analyze clinical data metrics and generate reports for decision-making.• Strong written and verbal communication skills.Salary InsightsAssociate Manager – Clinical Data Management roles in India typically offer salaries ranging from ₹18 LPA to ₹28 LPA, depending on experience, leadership responsibilities, and expertise in clinical data systems.Company OverviewKenvue is a global consumer health company known for its trusted healthcare brands and commitment to science-driven innovation. The organization develops and markets well-known healthcare and personal care products including Neutrogena, Aveeno, Tylenol, Listerine, Johnson's, and Band-Aid.With a strong heritage in consumer healthcare and a focus on science-based innovation, the company operates globally and serves millions of consumers through its health and wellness products.FAQs• What does a Clinical Data Management Associate Manager do?This role oversees the management of clinical trial data, ensuring data accuracy, quality, and compliance with regulatory standards.• What systems are commonly used in clinical data management?Professionals typically work with Electronic Data Capture systems and Clinical Data Management Systems.• Is vendor management part of this role?Yes, the role includes oversight of external vendors and CRO partners responsible for data management deliverables.• What career growth opportunities exist?Professionals may advance to roles such as Clinical Data Management Manager, Director of Data Management, or Head of Clinical Data Operations.Application Tips• Highlight experience in clinical data management systems and electronic data capture platforms.• Emphasize knowledge of regulatory standards such as ICH guidelines and Good Clinical Practice.• Showcase experience coordinating cross-functional clinical research teams.• Demonstrate experience managing vendor relationships and project timelines.• Include examples of clinical studies or data management projects you have supported.

Why This Role MattersData-driven insights are becoming increasingly important in the healthcare and medical technology industries. Organizations rely on healthcare data analytics to understand market trends, evaluate product performance, and make informed strategic decisions. The role of an Associate Healthcare Research & Data Analyst supports these objectives by analyzing healthcare datasets and generating insights that help companies navigate complex MedTech markets.Medical device companies and healthcare organizations depend on accurate data and market intelligence to understand customer demand, identify growth opportunities, and remain competitive in global markets. Analysts working in this domain play a vital role in interpreting large datasets and transforming them into actionable insights. The position also contributes to market research initiatives that evaluate industry trends, product positioning, and competitive landscapes. Through primary and secondary research, analysts help organizations understand the evolving needs of healthcare providers, patients, and regulatory environments. Another key aspect of the role involves maintaining and improving healthcare datasets used for forecasting and market modeling. Ensuring data quality and accuracy is critical for generating reliable insights and supporting business decision-making. For graduates from pharmacy, biotechnology, life sciences, or medical technology backgrounds, this role offers a unique opportunity to combine scientific knowledge with data analytics and market research skills. It also provides exposure to global healthcare markets and consulting projects within the MedTech sector. Overall, the Associate Healthcare Research & Data Analyst contributes to building data-driven healthcare intelligence that supports innovation, strategic planning, and improved healthcare solutions worldwide.Job DescriptionThe Associate Healthcare Research & Data Analyst works within the healthcare analytics and market research team to analyze data related to medical devices and healthcare markets. The role involves collecting, organizing, and interpreting healthcare datasets to generate insights that support market analysis and strategic decision-making. Professionals in this role work closely with data analysts, product managers, and subject matter experts to maintain healthcare databases and develop analytical models that track market performance and product trends. The position requires conducting both primary and secondary market research to gather information about healthcare technologies, medical device markets, and competitive landscapes. Analysts use this information to support forecasting models and provide strategic insights to clients and internal teams. Another important responsibility involves maintaining product catalogs and healthcare datasets used for market intelligence platforms. Analysts identify inconsistencies in data and ensure that information remains accurate, complete, and up to date. The role also includes preparing analytical reports and presentations that communicate insights to stakeholders, including consulting teams, clients, and senior management. Overall, the position combines healthcare research, data analytics, and market intelligence to support informed decision-making within the medical technology industry.Key Features of the Role:• Entry-level opportunity in healthcare data analytics and MedTech market research.• Exposure to global medical device and healthcare markets.• Opportunity to work with large real-world healthcare datasets.• Involvement in market research and competitive intelligence projects.• Collaboration with international healthcare analytics and consulting teams.• Opportunity to develop skills in data analysis, forecasting, and market modelling.• Hybrid work environment supporting professional development and collaboration.• Career growth opportunities in healthcare analytics and consulting.Responsibilities• Analyze healthcare and medical device datasets to generate market insights.• Conduct primary and secondary research related to healthcare and MedTech markets.• Perform competitive intelligence analysis for medical device companies.• Build and maintain datasets used for forecasting and market modeling.• Design and analyze surveys related to healthcare products and markets.• Maintain product catalog and SKU databases for medical device markets.• Identify trends, patterns, and strategic insights from healthcare data.• Resolve data inconsistencies and improve data quality within healthcare datasets.• Prepare analytical reports and presentations for internal teams and clients.• Collaborate with product managers, subject matter experts, and consulting teams.• Support the development of healthcare analytics products and platforms.Required Qualifications• Strong analytical and data interpretation skills.• Ability to work with large datasets and generate meaningful insights.• Strong communication and presentation skills.• Ability to manage multiple projects and meet deadlines.Educational Requirements• Bachelor of Pharmacy (B.Pharm)• Master of Pharmacy (M.Pharm)• B.E in Biotechnology or Medical Electronics• M.Sc in Biotechnology or Life Sciences• Other related healthcare or science degreesExperience and Skills• Freshers or candidates with up to 6 months of experience can apply.• Knowledge of SQL or Python for data analysis is desirable.• Strong proficiency in Microsoft Excel for data analysis and reporting.• Understanding of healthcare datasets and market research methodologies.• Ability to analyze large datasets and identify trends and patterns.• Strong written and verbal communication skills.• Ability to collaborate effectively within cross-functional teams.• Good organizational skills and attention to detail.Salary InsightsEntry-level healthcare research and data analyst roles in India typically depending on educational background, technical skills, and analytical expertise. Candidates with strong data analysis skills such as SQL, Python, or advanced Excel may receive higher compensation packages.Company OverviewClarivate is a global provider of trusted insights and analytics that help organizations accelerate innovation. The company supports industries including life sciences, healthcare, academia, and intellectual property through advanced data analytics, research platforms, and consulting services. Within its healthcare division, Clarivate provides market intelligence and analytics solutions to pharmaceutical and medical device companies, enabling them to make strategic decisions based on reliable data and industry insights.FAQs• What does a Healthcare Research & Data Analyst do?A Healthcare Research & Data Analyst analyzes healthcare datasets, conducts market research, and generates insights for medical device and healthcare companies.• Is programming knowledge required for this role?Basic knowledge of SQL or Python is beneficial but may not always be mandatory for entry-level roles.• What industries does this role support?The role primarily supports medical device companies, healthcare organizations, and life sciences businesses.• What career growth opportunities exist?Professionals may advance to roles such as Senior Healthcare Analyst, Healthcare Data Scientist, or Healthcare Consulting Specialist.Application Tips• Highlight analytical skills and experience working with datasets.• Emphasize proficiency in Microsoft Excel, SQL, or Python.• Showcase any academic or internship experience in healthcare research or market analysis.• Demonstrate strong communication and presentation abilities.• Include examples of data analysis projects or research work in your resume.

Why This Role MattersPharmacovigilance professionals play an essential role in safeguarding patient health by monitoring the safety of medicines and ensuring timely reporting of adverse events. Accurate safety data collection, evaluation, and reporting are crucial to maintaining regulatory compliance and protecting patients worldwide.The Japan Local Case Advisor role at AstraZeneca is particularly important because it focuses on managing safety reports related to products used in the Japanese market. The position supports Individual Case Safety Report processing, adverse event reporting, and compliance with Japanese pharmacovigilance regulations.Working within the Global Business Services Patient Safety team, the role involves collaborating with global safety teams while ensuring that local Japanese regulatory requirements are met. This includes managing safety cases, performing data entry into safety databases, and supporting pharmacovigilance compliance activities. For professionals with pharmacovigilance experience and Japanese language proficiency, this role provides a unique opportunity to contribute to global drug safety programs while supporting patient safety initiatives for important therapeutic products.Job DescriptionAstraZeneca is seeking a Japan Local Case Advisor to support pharmacovigilance operations within the Global Business Services Patient Safety function.The selected candidate will be responsible for managing Individual Case Safety Reports and supporting safety reporting activities related to AstraZeneca and Rare Disease Unit products in Japan. The role requires proficiency in English and Japanese and involves collaboration with internal safety teams to ensure timely and accurate safety data processing. This position involves case intake activities, safety database data entry, regulatory compliance monitoring, and support for audits and inspections. The role also contributes to maintaining pharmacovigilance quality systems and ensuring adherence to Japanese regulatory standards.Key Features of the RoleOpportunity to work in global pharmacovigilance and patient safety operationsExposure to safety reporting for the Japanese pharmaceutical marketInvolvement in Individual Case Safety Report management and adverse event reportingCollaboration with multinational teams in a global pharmaceutical environmentParticipation in pharmacovigilance quality systems and compliance activitiesOpportunity to contribute to safety monitoring for innovative medicinesResponsibilitiesCase Intake and Safety ReportingAccept and validate safety reports for domestic cases in Japan and conduct preliminary case assessments. Communicate with reporters when necessary to collect additional safety information and ensure the accuracy of safety reports. Ensure proper handling of personal and confidential information in accordance with regulatory requirements and company policies. Perform routine quality checks and initiate follow-up activities when additional information is required. Collaborate with internal teams to clarify case details, triage incoming safety reports, and escalate urgent or reportable cases for further investigation.Safety Data Entry and Case ManagementEnter safety data accurately into pharmacovigilance databases and ensure that all relevant information is documented correctly. Work with internal teams to resolve data entry issues and ensure high-quality safety documentation. Initiate follow-up requests using product or event-specific questionnaires to obtain additional safety information when required.Audit and Inspection SupportMaintain pharmacovigilance documentation in accordance with internal procedures and regulatory requirements. Support internal and external audits and assist with regulatory authority inspections by ensuring inspection-ready documentation.Regulatory ComplianceEnsure compliance with Japanese regulatory standards for Individual Case Safety Reports and adverse event reporting. Identify urgent or high-risk cases and escalate them according to established safety procedures.Quality Management System SupportContribute to the effective implementation of the pharmacovigilance Quality Management System and maintain awareness of regulatory changes related to the Japanese pharmaceutical market.General ResponsibilitiesPerform peer reviews of safety cases and support additional pharmacovigilance projects when required. Collaborate with internal teams on pharmacovigilance aspects related to organized data collection programs.Required QualificationsEducational RequirementsBachelor’s degree in Life Sciences, Pharmacy, Medicine, or a related scientific field.Experience and Skills1 to 2 years of experience working with safety databases or pharmacovigilance data entry. Strong attention to detail and the ability to identify sensitive personal or confidential information in safety reports. Experience working collaboratively with cross-functional teams and the ability to resolve operational issues effectively.Language RequirementsJapanese language proficiency at N2 level or higher for listening, writing, and speaking. Reading proficiency in Japanese medical terminology and Kanji characters at N3 to N1 level. English language proficiency equivalent to A2 level according to the CEFR framework.Technical KnowledgeFamiliarity with pharmacovigilance processes and adverse event reporting standards. Experience with safety databases such as Oracle Argus Safety is preferred. Knowledge of global pharmacovigilance guidelines such as Good Pharmacovigilance Practice and Good Clinical Practice is considered advantageous. Understanding of medical coding systems such as MedDRA and WHO Drug Dictionary is beneficial.Professional SkillsStrong problem-solving and analytical abilities. Excellent written and verbal communication skills. Ability to work effectively in multicultural teams and collaborate with stakeholders across different regions.Salary InsightsAlthough the exact salary package has not been disclosed, pharmacovigilance roles within global pharmaceutical companies typically offer competitive compensation based on experience, skills, and regional policies. Employees may also benefit from professional development opportunities, exposure to global pharmacovigilance operations, and participation in international patient safety initiatives.Company OverviewAstraZeneca is a global biopharmaceutical company focused on discovering, developing, and delivering innovative medicines that transform patient care. The company operates across multiple therapeutic areas including oncology, cardiovascular diseases, respiratory conditions, and rare diseases. AstraZeneca places strong emphasis on patient safety and regulatory compliance, supported by advanced pharmacovigilance systems and global safety monitoring programs. Through collaborative research, advanced technology, and strong global partnerships, AstraZeneca continues to develop life-changing medicines while maintaining high standards of quality and safety.FAQsWho can apply for this role?Candidates with a life sciences background and pharmacovigilance experience, along with Japanese language proficiency.Is Japanese language proficiency mandatory?Yes. Japanese language skills at N2 level or higher are required for handling domestic safety cases in Japan.What type of work does the Japan Local Case Advisor perform?The role involves case intake, safety data entry, adverse event reporting, regulatory compliance monitoring, and audit support.Is experience with safety databases required?Experience with pharmacovigilance safety databases such as Argus is preferred.Application TipsHighlight your pharmacovigilance or safety data management experience in your resume.Mention your proficiency in Japanese language and experience working with Japanese regulatory requirements.Include experience with safety databases and adverse event reporting systems.Demonstrate your attention to detail and ability to handle confidential information responsibly.Showcase your ability to collaborate with global teams and manage safety case documentation accurately.

Why This Role MattersMedical data abstraction plays a crucial role in healthcare analytics, clinical research, and real-world evidence generation. Data abstractors review medical records and extract clinically relevant information to support research studies, healthcare analytics, and evidence-based medical insights.The Medical Data Abstractor role focuses on reviewing electronic medical records, identifying relevant clinical information, and entering structured data into electronic systems. By accurately extracting patient information such as diagnoses, treatments, adverse events, and medication details, professionals in this role contribute to high-quality healthcare data used in clinical research and healthcare decision-making.This position is particularly important in areas such as oncology, cardiovascular diseases, and metabolic disorders where detailed patient data is required for clinical analysis and research. For candidates with medical or healthcare backgrounds, the role offers an opportunity to work with real-world clinical data while contributing to healthcare analytics and research initiatives.Job DescriptionThe organization is seeking Medical Data Abstractors to support clinical data abstraction and medical record review activities at its Bangalore location.The selected candidate will navigate electronic medical record systems, review patient records, and extract relevant clinical data according to project-specific requirements. The role involves understanding medical reports, identifying relevant clinical information, and entering accurate data into designated electronic databases. Medical Data Abstractors will also collaborate with project teams, respond to queries from project leads, and contribute to continuous improvement of data abstraction processes.Key Features of the Role• Opportunity to work in medical data abstraction and healthcare analytics• Exposure to electronic medical record systems and clinical databases• Involvement in reviewing patient medical records and clinical documentation• Participation in healthcare data projects across multiple therapeutic areas• Collaboration with healthcare analytics and clinical research teams• Opportunity to develop expertise in real-world healthcare data analysisResponsibilitiesMedical Record Review• Access electronic medical record systems and other medical databases to review patient records• Identify and extract relevant medical information according to project-specific requirements• Understand diagnostic reports, pathology reports, and clinical documentation to obtain accurate dataClinical Data Abstraction• Enter extracted clinical data into designated electronic data systems• Categorize information related to inclusion and exclusion criteria, adverse events, hospitalizations, and medications• Ensure data accuracy and consistency during abstraction activitiesProject Familiarization and Knowledge Development• Review project-specific documentation to understand study objectives and abstraction requirements• Use available resources to build medical knowledge relevant to assigned projects• Stay updated with project procedures and abstraction guidelinesTeam Collaboration and Knowledge Sharing• Share medical knowledge and project-specific procedural information with other data abstractors• Participate in periodic team meetings and contribute to abstraction workflow discussions• Support team members with project-related queries when requiredQuery Resolution and Communication• Respond promptly to queries raised by lead abstractors, operations managers, or project teams• Clarify clinical data discrepancies when reviewing medical records• Ensure communication with project personnel regarding abstraction tasks and updatesAdditional Responsibilities• Assist in reviewing medical records to assess eligibility for new projects• Support ongoing improvements in data abstraction processes and workflowsRequired QualificationsEducational Requirements• BDS or MDS (Oral Pathology, Oral Medicine, or Public Health Dentistry)• B.Sc Nursing or M.Sc NursingExperience and Skills• 0 to 4 years of experience in medical record review, healthcare data abstraction, or clinical documentation analysis• Strong understanding of medical terminology and clinical documentation• Ability to interpret diagnostic reports, pathology reports, and patient treatment records• Knowledge of clinical concepts such as adverse events, medications, and hospitalization data• Experience reviewing medical records or patient treatment data is preferredPreferred Knowledge• Oncology experience or understanding of cancer diagnosis, treatment, and recovery processes• Familiarity with medical data related to therapeutic areas such as cardiovascular, immunology, and metabolic diseasesTechnical Skills• Strong computer skills and ability to work with electronic data systems• Familiarity with medical record databases and healthcare data platforms• Ability to learn and adapt to new software systems and digital toolsProfessional Skills• Strong critical thinking and analytical abilities• Excellent organizational and time-management skills• Ability to work independently and make informed decisions when abstracting data• Flexibility to adapt to changing project requirements and work schedulesSalary InsightsAlthough the exact salary is not specified, Medical Data Abstractor roles in healthcare analytics and clinical data services typically offer competitive compensation depending on experience, qualifications, and project complexity. Additional benefits may include exposure to healthcare data analytics projects, professional development opportunities, and experience working with real-world medical data.Company OverviewConcertAI is a healthcare analytics and data science company that leverages real-world medical data to support clinical research, healthcare decision-making, and drug development. The organization collaborates with healthcare providers, life sciences companies, and research institutions to generate valuable insights from clinical data. By combining advanced data analytics with medical expertise, ConcertAI helps improve healthcare outcomes, accelerate clinical research, and support evidence-based medical innovation.FAQsWho can apply for this role?Candidates with BDS, MDS (Oral Pathology, Oral Medicine, or Public Health Dentistry), B.Sc Nursing, or M.Sc Nursing qualifications.What experience is required for this position?Applicants with 0 to 4 years of experience in medical data review, clinical documentation analysis, or healthcare data abstraction can apply.What type of work will the Medical Data Abstractor perform?The role involves reviewing medical records, extracting clinical information, and entering structured data into electronic databases.Is oncology experience required?Oncology experience is preferred but not mandatory. Knowledge of other therapeutic areas such as cardiovascular or immunology is also considered.Are computer skills required for this role?Yes. Since most tasks involve reviewing electronic records and entering data into digital systems, strong computer skills are essential.Application Tips• Highlight experience reviewing medical records or clinical documentation• Mention knowledge of medical terminology and patient treatment data• Demonstrate ability to interpret diagnostic and pathology reports• Showcase experience working with electronic medical record systems or healthcare databases• Emphasize analytical skills and attention to detail when handling clinical data

Why This Role MattersPharmacovigilance is a critical function in the pharmaceutical and biopharmaceutical industry, ensuring that medicines remain safe and effective throughout their lifecycle. From clinical trials to post-marketing surveillance, pharmacovigilance professionals monitor adverse events, analyze safety data, and ensure regulatory compliance with international drug safety standards.The Senior Pharmacovigilance Specialist role at Alvotech is essential in maintaining the safety profile of biosimilar medicines and supporting global safety operations. The position focuses on safety data management for clinical trials and post-marketing programs while ensuring that pharmacovigilance activities meet international regulatory requirements. As part of the Global Safety Data Management team, the Senior PV Specialist will contribute to safety data analysis, adverse event reporting, regulatory submissions, and the development of pharmacovigilance processes and systems. The role also supports safety system lifecycle management and cross-functional collaboration with clinical, regulatory, and quality teams.This position provides experienced pharmacovigilance professionals with the opportunity to work on global drug safety programs while contributing to the development and monitoring of biosimilar medicines.Job DescriptionAlvotech is seeking a skilled Senior Pharmacovigilance Specialist to support clinical safety and post-marketing pharmacovigilance activities within its Research and Development function. The selected candidate will join the Global Safety Data Management team and will be responsible for managing safety data related to clinical trials and marketed products. The role involves overseeing adverse event reporting, maintaining safety databases, ensuring regulatory compliance, and supporting the development of pharmacovigilance systems and processes.The Senior PV Specialist will also collaborate with cross-functional teams across the organization to ensure that safety activities are performed efficiently and in compliance with global pharmacovigilance standards.Key Features of the Role• Opportunity to work in global pharmacovigilance and safety data management• Involvement in clinical trial safety monitoring and post-marketing surveillance• Participation in pharmacovigilance system configuration and lifecycle management• Collaboration with global regulatory, quality, and clinical teams• Contribution to safety process optimization and regulatory compliance initiatives• Exposure to safety monitoring for biosimilar medicinesResponsibilitiesClinical Safety & Pharmacovigilance Activities• Manage assigned clinical safety and post-marketing pharmacovigilance activities• Handle Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) processing• Support regulatory safety submissions and reporting requirements• Conduct literature monitoring and digital platform monitoring for safety signals• Perform pharmacovigilance reconciliations and safety data reviews• Support activities related to EudraVigilance and XEVMPDSafety Systems & Data Management• Participate in configuration, validation, and lifecycle management of pharmacovigilance systems• Maintain and monitor safety databases to ensure data accuracy and regulatory compliance• Work with safety systems such as Oracle Argus Safety, ARISg Safety System, and Veeva Vault SafetyPharmacovigilance Process Management• Create, maintain, and optimize global pharmacovigilance processes• Ensure compliance with international regulatory guidelines and company procedures• Monitor pharmacovigilance activities to maintain regulatory compliance across clinical and post-marketing programsCross-Functional Collaboration• Work closely with pharmacovigilance teams involved in benefit-risk management and clinical trials• Collaborate with departments such as Quality, Regulatory Affairs, IT, and Clinical Program Development• Coordinate with external pharmacovigilance service providers and business partnersTraining, Audits & Compliance• Deliver pharmacovigilance training programs to internal staff and external partners• Participate in safety-related audits and regulatory inspections• Ensure proper documentation and compliance with global pharmacovigilance standardsRequired QualificationsEducational Requirements• Master’s degree in Pharmaceutical Sciences, Pharmacy, Medicine, or Life SciencesExperience and Skills• Minimum 5 years of experience in Pharmacovigilance or Drug Safety• Strong experience in safety data management functions• Hands-on experience in clinical trial safety and post-marketing pharmacovigilance activities• Experience working with global pharmaceutical products and clinical trials• Familiarity with biologic or combination products is considered an advantageTechnical Knowledge• Experience working with pharmacovigilance safety systems such as Oracle Argus Safety, ARISg Safety System, or Veeva Vault Safety• Understanding of global pharmacovigilance regulations including• ICH Guidelines• FDA Regulations• Good Pharmacovigilance Practices• Good Clinical Practice• Council for International Organizations of Medical Sciences safety reporting standardsProfessional Skills• Strong analytical, organizational, and time-management skills• Excellent communication and stakeholder management abilities• Ability to work independently and manage complex pharmacovigilance activities• Comfortable working in global and multicultural teamsSalary InsightsAlthough the salary package has not been specified, Senior Pharmacovigilance Specialist roles in the global biopharmaceutical industry typically offer competitive compensation based on experience, expertise, and geographic location.Additional benefits may include international project exposure, professional development opportunities, and involvement in global clinical safety programs.Company OverviewAlvotech is a global specialty biopharmaceutical company dedicated to developing and manufacturing high-quality biosimilar medicines.The company focuses exclusively on biosimilars with the goal of improving access to biologic treatments while maintaining strict regulatory and quality standards. Within the Research and Development function, the Integrated Clinical and Medical Research department develops clinical strategies aligned with biosimilar regulatory guidelines and health authority requirements. Through advanced safety monitoring systems and global pharmacovigilance operations, Alvotech ensures the safety, effectiveness, and regulatory compliance of its products worldwide.FAQsWho can apply for this role?Candidates with a Master’s degree in Pharmacy, Life Sciences, or Medicine and at least 5 years of pharmacovigilance experience.What type of work does the Senior PV Specialist perform?The role includes adverse event management, safety data analysis, regulatory reporting, safety system management, and pharmacovigilance compliance activities.Is experience with safety databases required?Yes. Experience with systems such as Argus, ARISg, or Veeva Vault Safety is preferred.Does the role involve working with clinical trials?Yes. The position supports safety monitoring for both clinical trials and post-marketing pharmacovigilance programs.Application Tips• Highlight your pharmacovigilance and safety data management experience• Mention expertise in ICSR processing, SAE reporting, and regulatory submissions• Include knowledge of safety databases such as Argus or Veeva Vault Safety• Demonstrate familiarity with global PV regulations such as ICH, GVP, and GCP guidelines• Emphasize strong documentation practices and cross-functional collaboration skills

Why This Role MattersPharmacovigilance plays a critical role in ensuring the safety of medicines throughout their lifecycle, from clinical trials to post-marketing surveillance. Drug safety professionals monitor adverse events, analyze safety data, and ensure compliance with global regulatory standards to protect patient health.The Pharmacovigilance Specialist role at Alvotech provides an excellent opportunity to work in global safety data management within the biopharmaceutical industry. The position supports safety monitoring for clinical trials and post-marketing programs while ensuring adherence to international pharmacovigilance regulations. As part of the Global Safety Data Management team, the specialist will contribute to safety systems, regulatory submissions, and pharmacovigilance process improvements. This role is especially important for biosimilar products, where rigorous safety monitoring and regulatory compliance are essential to ensure patient safety and product reliability.For professionals with pharmacovigilance experience, this role offers exposure to global safety operations, regulatory frameworks, and advanced safety systems used in modern drug safety management.Job DescriptionAlvotech is seeking a Pharmacovigilance Specialist to support clinical safety and post-marketing pharmacovigilance activities within its Research and Development function. The selected candidate will join the Global Safety Data Management team and work closely with safety leaders to ensure accurate management of safety data for clinical trials and marketed products. The role includes monitoring adverse events, managing safety reports, ensuring regulatory compliance, and supporting pharmacovigilance system operations.This position also contributes to developing pharmacovigilance processes, supporting audits and inspections, and collaborating with internal and external stakeholders involved in drug safety and regulatory activities.Key Features of the Role• Work within global pharmacovigilance and safety data management• Exposure to clinical trial safety monitoring and post-marketing surveillance• Involvement in safety system configuration and lifecycle management• Opportunity to collaborate with global regulatory and clinical teams• Participate in pharmacovigilance process development and compliance initiatives• Contribute to safety monitoring for biosimilar pharmaceutical productsResponsibilitiesClinical Safety & Pharmacovigilance Activities• Manage assigned clinical safety and post-marketing pharmacovigilance activities• Handle Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) management• Support regulatory safety submissions and reporting requirements• Conduct literature monitoring and digital platform monitoring for safety signals• Perform pharmacovigilance reconciliations and safety data verification• Support activities related to EudraVigilance and XEVMPDSafety Systems & Data Management• Support configuration, validation, and lifecycle management of pharmacovigilance systems• Maintain safety databases and ensure accurate safety data management• Work with safety systems such as Oracle Argus Safety, ARISg Safety System, and Veeva Vault SafetyPharmacovigilance Process Management• Develop and maintain global pharmacovigilance procedures and workflows• Ensure compliance with international regulatory guidelines and internal SOPs• Monitor safety processes to maintain regulatory compliance across clinical programsCross-Functional Collaboration• Collaborate with pharmacovigilance teams involved in benefit-risk assessment and clinical safety• Work with internal departments such as Quality, Regulatory Affairs, IT, and Clinical Program Development• Coordinate with external pharmacovigilance service providers and business partnersTraining, Audits & Compliance• Deliver pharmacovigilance training to internal staff and external stakeholders• Support safety-related audits and regulatory inspections• Ensure documentation and processes meet global regulatory requirementsRequired QualificationsEducational Requirements• Master’s degree in Pharmaceutical Sciences, Pharmacy, Medicine, or Life SciencesExperience and Skills• Minimum 3 years of experience in Pharmacovigilance or Drug Safety• Experience working in safety data management functions• Hands-on experience in clinical trial safety and post-marketing pharmacovigilance• Knowledge of safety databases such as Argus, ARISg, or Veeva Vault Safety• Experience working with global pharmaceutical products and clinical trials• Familiarity with biologic or combination products is an advantageRegulatory Knowledge• Strong understanding of global pharmacovigilance regulations and guidelines including• ICH Guidelines• FDA Regulations• GVP Guidelines• GCP Guidelines• CIOMS GuidelinesProfessional Skills• Strong organizational and time-management skills• Excellent communication and interpersonal abilities• Ability to work independently and manage multiple safety activities• Capability to collaborate effectively in multicultural and global teamsSalary InsightsAlthough the exact salary has not been disclosed, Pharmacovigilance Specialist roles in the global biopharmaceutical industry typically offer competitive compensation based on experience, expertise, and geographic location. Additional benefits may include international exposure, professional development opportunities, and involvement in global clinical programs for biosimilar medicines.Company OverviewAlvotech is a fully integrated specialty biopharmaceutical company dedicated to the development and manufacturing of high-quality biosimilar medicines.The company focuses on improving patient access to biologic treatments by developing cost-effective biosimilars while maintaining strict regulatory and quality standards. Within its Research and Development division, the Integrated Clinical and Medical Research department develops strategies aligned with global biosimilar guidelines and regulatory authority requirements. Through innovative clinical programs and strong pharmacovigilance systems, Alvotech ensures the safety, effectiveness, and regulatory compliance of its products worldwide.FAQsWho can apply for this role?Candidates with a Master’s degree in Pharmacy, Life Sciences, or Medicine and at least 3 years of pharmacovigilance experience.What type of work will the PV Specialist perform?The role includes clinical safety monitoring, adverse event management, safety data analysis, regulatory submissions, and pharmacovigilance system management.Is experience with safety databases required?Yes. Experience with safety systems such as Argus, ARISg, or Veeva Vault Safety is highly preferred.Does the role involve working with clinical trials?Yes. The role involves safety monitoring for clinical trials and post-marketing programs.Application Tips• Highlight your pharmacovigilance experience and safety data management expertise• Mention experience working with safety databases such as Argus or Veeva Vault Safety• Include knowledge of global PV regulations such as ICH, GVP, and GCP guidelines• Demonstrate experience managing ICSRs, SAE reporting, and safety monitoring• Emphasize your ability to collaborate with global teams and maintain regulatory compliance

Why This Role MattersPharmacovigilance and post-market safety monitoring are essential for protecting consumers and ensuring that healthcare and wellness products remain safe after they reach the market. Safety professionals play a critical role in analyzing adverse event data, identifying potential risks, and ensuring compliance with global regulatory requirements.The Senior Associate – Global Market Vigilance (GMV) position at Unilever within Unilever R&D Bangalore offers an excellent opportunity for experienced pharmacovigilance professionals to contribute to consumer safety initiatives across global markets. Working under the Global Regulatory Affairs function of the Wellbeing Collective, the role focuses on safety data analytics, signal detection, adverse event monitoring, and compliance reporting. By transforming complex safety datasets into actionable insights, the Senior Associate supports proactive risk management and helps ensure that consumer products meet the highest safety standards. This role is particularly important because it supports end-to-end post-market surveillance activities, helping organizations identify emerging safety signals early and take appropriate action to protect consumers worldwide.Job DescriptionUnilever is seeking a Senior Associate – Global Market Vigilance to support pharmacovigilance and safety monitoring activities for products managed by the Wellbeing Collective. The selected candidate will analyze adverse event data, identify safety trends, build dashboards, and support regulatory reporting processes. The role requires strong analytical expertise and hands-on experience working with safety databases such as Veeva Vault Safety. The position also requires collaboration with cross-functional teams across regulatory affairs, R&D, quality assurance, and consumer care to maintain data integrity, regulatory compliance, and proactive safety monitoring.Key Features of the Role• Work within Global Regulatory Affairs and pharmacovigilance operations• Focus on safety data analytics, signal detection, and trend monitoring• Use advanced safety databases such as Veeva Vault Safety• Collaborate with cross-functional teams including R&D, Quality, and Regulatory Affairs• Contribute to global post-market surveillance and consumer safety programs• Opportunity to mentor junior team members and support analytics initiativesResponsibilitiesSafety Data Analytics, Trending & Signal Detection• Lead trending and signal detection activities across global adverse event datasets• Conduct quantitative and qualitative analysis of safety data to identify emerging risks• Develop dashboards, safety scorecards, and trend reports for stakeholders• Use statistical and analytical tools to generate predictive insights and early warning indicators• Support signal validation and risk assessment for potential safety concerns• Collaborate with analytics teams to improve data automation and visualizationCase Management & Compliance• Manage intake, triage, and documentation of adverse event complaints using Veeva Vault Safety• Perform causality and seriousness assessments for safety events• Ensure timely escalation of potential serious adverse events• Conduct duplicate checks and maintain data quality reviews• Maintain compliance with global adverse event reporting standards and internal SOPsSystem & Process Optimization• Support configuration and validation of safety database updates• Recommend improvements to enhance safety analytics readiness and data accuracy• Conduct audits and reconciliation of safety dataCross-functional Collaboration & Leadership• Act as a point of contact for Regulatory Affairs, R&D, Quality, and customer experience teams• Present safety insights and risk indicators in cross-functional meetings• Mentor junior team members on analytics methods and case processing• Support corrective and preventive actions related to safety operationsReporting & Insights• Generate and review safety reports, dashboards, and KPI summaries• Interpret safety data and develop analytical insights• Support regulatory submissions and product safety reviews• Provide recommendations based on safety trend analysisRequired QualificationsEducational Requirements• Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or a related fieldExperience and Skills• 5–8 years of experience in pharmacovigilance or drug safety• Hands-on experience with safety databases such as Veeva Vault Safety• Strong knowledge of MedDRA coding standards• Experience with global adverse event reporting requirements• Demonstrated expertise in safety data analytics, signal detection, and dashboard development• Strong analytical and problem-solving abilities• Ability to communicate complex safety insights clearly to stakeholdersSalary InsightsWhile the exact salary package has not been disclosed, senior pharmacovigilance roles in Bangalore with 5–8 years of experience typically offer competitive compensation depending on expertise and company standards.Common benefits may include competitive pay, performance incentives, professional development opportunities, exposure to global safety operations, and career advancement within regulatory affairs and pharmacovigilance.Company OverviewUnilever is one of the world’s leading consumer goods companies, operating in more than 190 countries and serving billions of consumers every day. The organization develops products across categories such as nutrition, personal care, and wellbeing.Through Unilever R&D Bangalore, the company drives research, innovation, and regulatory excellence for global markets. The Global Regulatory Affairs team ensures that products meet strict safety standards while maintaining consumer trust and regulatory compliance. Unilever is also recognized for its commitment to sustainability, diversity, and inclusive workplace practices.FAQsWho can apply for this role?Professionals with 5–8 years of pharmacovigilance experience and a degree in Pharmacy or Life Sciences.Is experience with Veeva Vault Safety required?Yes. Hands-on experience with Veeva Vault Safety or similar pharmacovigilance databases is preferred.What type of work will this role involve?The role focuses on safety data analytics, signal detection, adverse event management, and regulatory reporting.Is this a leadership role?Although it is an individual contributor role, the position involves mentoring junior staff and collaborating with multiple cross-functional teams.Application Tips• Highlight your pharmacovigilance experience and safety analytics expertise• Mention your experience with Veeva Vault Safety or other safety databases• Include knowledge of MedDRA coding and global adverse event reporting standards• Showcase experience in safety dashboards, signal detection, or data analytics projects• Emphasize your ability to analyze complex datasets and communicate insights clearly to stakeholders.

Why This Role MattersThe General Dentist plays an important role in maintaining patients’ oral health by diagnosing dental conditions, performing routine dental procedures, and educating patients about proper oral hygiene. This role helps ensure accessible and quality dental care while building strong patient relationships within the community.Job DescriptionHealthy Dental Clinicv is seeking a General Dentist for a full-time or part-time on-site role in Bengaluru. The selected candidate will provide comprehensive dental care, perform common dental procedures, and communicate effectively with patients to ensure a positive clinical experience at the clinic located near Old Madras Road.Key Features of the Role• Position: General Dentist• Company: Healthy Dental Clinicv• Location: Bangalore City, Bengaluru, Karnataka, India• Employment Type: Full-Time or Part-Time• Workplace Type: On-site• Salary: ₹20,000 – ₹40,000 per month• Expected Work Hours: Approximately 48 hours per weekResponsibilities• Diagnose dental issues through patient examinations and assessments• Perform basic dental procedures such as root canal treatments (RCT), fillings, crown preparations, and simple extractions• Provide patient consultations and develop appropriate treatment plans• Educate patients on oral hygiene and preventive dental care• Maintain accurate patient records and treatment documentation• Ensure proper sterilization and compliance with dental safety protocols• Use basic computer systems for patient records and clinic management• Communicate effectively with patients to ensure a comfortable treatment experienceRequired Qualification• Bachelor of Dental Surgery (BDS) or equivalent dental qualification from a recognized institutionImportant Requirements• Strong knowledge of basic dental procedures including RCT, extractions, fillings, and crown preparation• Good patient communication and interpersonal skills• Basic computer skills for clinic documentation and workflow• Proficiency in English and Kannada or Telugu• Ability to work effectively in a clinical team environmentWhat We Offer• Opportunity to work in a reputed dental clinic environment• Flexible employment options (full-time or part-time)• Competitive salary based on experience and skills• Opportunity to build clinical experience in general dentistry• Supportive workplace environmentExperience and Skills• General dentistry procedures• Root canal treatments (RCT)• Crown preparation and restorative dentistry• Dental extractions and fillings• Patient consultation and treatment planning• Clinical documentation and computer-based record managementSalary Insights• Monthly Salary: ₹20,000 – ₹40,000• Salary may vary depending on experience, clinical skills, and working hoursCompany OverviewHealthy Dental Clinicv is a dental clinic located in Bengaluru that focuses on providing comprehensive and accessible dental care services. The clinic offers a range of routine and restorative dental treatments while prioritizing patient comfort, quality care, and professional clinical practices.FAQsWhat qualification is required for this role?Candidates must have a Bachelor of Dental Surgery (BDS) or an equivalent dental qualification.What procedures will the General Dentist perform?The dentist will perform procedures such as root canal treatments, simple extractions, fillings, and crown preparations.Is this a full-time or part-time job?The clinic offers both full-time and part-time employment options.What languages are preferred for this role?Candidates should be proficient in English and Kannada or Telugu.Application Tips• Highlight experience performing RCT, fillings, and crown preparations• Mention strong patient communication skills• Include any experience using digital systems or dental software• Emphasize proficiency in English and Kannada or Telugu• Showcase experience in general dentistry procedures

Why This Role MattersMedical Affairs professionals play a vital role in connecting scientific knowledge with clinical practice, regulatory compliance, and commercial strategy. They ensure that pharmaceutical products are supported by accurate scientific evidence, regulatory documentation, and meaningful engagement with healthcare professionals.Job DescriptionPharmed Limited is hiring an Assistant Manager – Medical Affairs in Bangalore, Karnataka. This role involves medical writing, regulatory support, clinical research coordination, and collaboration with healthcare professionals and key opinion leaders (KOLs). The position is suitable for professionals with experience in pharmaceutical medical affairs, regulatory submissions, and scientific communication.Key Features of the Role• Position: Assistant Manager – Medical Affairs• Company: Pharmed Limited• Location: Bangalore, Karnataka, India• Industry: Pharmaceutical / Medical Affairs• Employment Type: Full-Time• Experience Required: 6 Months – 3 YearsResponsibilities• Support preparation of regulatory dossiers for new product submissions and respond to regulatory authority queries such as CDSCO.• Prepare and present regulatory submissions to advisory or expert committees when required.• Develop and maintain FSSAI product dossiers for regulatory and customer inquiries.• Track regulatory developments and present updates to management.• Respond to product-related medical queries from healthcare professionals and the marketing team.• Review and approve medical content used in brand promotional materials and digital marketing.• Develop monographs, training manuals, and CME slide decks for product launches.• Review scientific literature and prepare study summaries for management and marketing teams.• Develop scientific presentations for medical education programs and CMEs.• Conduct surveys and market research on new product concepts with Key Opinion Leaders (KOLs).• Coordinate with KOLs and Contract Research Organizations (CROs) for clinical studies and manuscript writing.• Participate in planning and conducting clinical studies and trials.• Support pharmacovigilance activities including adverse event reporting, safety monitoring, and PSUR coordination.Required Qualification• Postgraduate degree in Pharmacy, Pharmacology, Pharmaceutics, Mac . Pharmacology, Pharm.D, or equivalent.Important Requirements• 6 months to 3 years of experience in Medical Affairs, Regulatory Affairs, or Medical Writing within the pharmaceutical industry.• Experience with CDSCO or FSSAI regulatory submissions is preferred.• GCP certification or pharmacovigilance training is an advantage.• Prior experience working with KOLs or CROs is beneficial.What We Offer• Opportunity to work in pharmaceutical medical affairs and regulatory functions.• Exposure to clinical research, regulatory submissions, and medical communication.• Collaboration with healthcare professionals, KOLs, and research organizations.Experience and Skills• Medical and scientific writing• Medico-marketing communication and content development• Regulatory dossier preparation (CDSCO, FSSAI)• Clinical research and trial coordination• Pharmacovigilance support and adverse event reporting• Proficiency in MS Office (Word, Excel, PowerPoint)• Strong analytical thinking and scientific literature interpretation• Excellent written and verbal communication skillsCompany OverviewPharmed Limited is a pharmaceutical organization involved in developing and supporting healthcare products through scientific research, regulatory compliance, and medical affairs initiatives. The company works closely with healthcare professionals and regulatory bodies to ensure product quality, safety, and effective communication of medical information.FAQsWhat qualification is required for this role?Candidates must have a postgraduate degree in Pharmacy, Pharmacology, Pharmaceutics, Pharm.D, or a related field.How much experience is required?The role requires 6 months to 3 years of experience in medical affairs, regulatory affairs, or medical writing.Where is the job located?The position is based in Bangalore, Karnataka, India.Does the role involve travel?Yes, occasional travel may be required for meetings with KOLs, CRO coordination, and scientific conferences.Application Tips• Highlight postgraduate qualifications in pharmacy or pharmacology.• Mention experience in regulatory submissions, medical writing, or clinical research.• Showcase knowledge of CDSCO and FSSAI regulations.• Emphasize skills in scientific communication and literature review.

Why This Role MattersAssociate Dentists play an important role in delivering quality dental care by assisting in diagnosis, performing basic dental procedures, and supporting patient treatment plans. In modern dental organizations, dentists also work with advanced technologies and collaborate with senior doctors to improve patient outcomes and clinical efficiency.Job DescriptionDezy is hiring an Associate Dentist to join its dental team in Bangalore, Karnataka. Dezy is a fast-growing dental health-tech company founded by IIT/IIM alumni and backed by leading investors. This role is suitable for freshers or dentists with up to 1 year of experience who are interested in working in a technology-driven dental care environment and gaining exposure to modern dental treatments.Key Features of the Role• Position: Associate Dentist• Company: Dezy• Location: Marathahalli, Vidyaranyapura, Jakkur – Bangalore City, Bengaluru, Karnataka, India• Industry: Health, Wellness & Fitness / Dental Care• Employment Type: Full-Time• Salary: ₹20,000 – ₹25,000 per month (with performance incentives)Responsibilities• Perform dental examinations and diagnose oral health conditions• Develop treatment plans in collaboration with senior dentists• Conduct basic dental procedures such as intraoral scans, cleanings, and fillings• Assist senior doctors during dental surgeries and complex procedures• Educate patients about oral hygiene, preventive care, and post-treatment care• Maintain accurate patient records, treatment plans, and medical histories• Coordinate with administrative teams to ensure smooth patient care• Call and coordinate with patients for home or partner clinic scan appointments• Upload scan files and intraoral/extraoral photos within the specified turnaround time• Participate in trade fairs and outreach activities to build relationships with dental clinics and professionals• Stay updated with advancements in dentistry including aligners and dental implantsRequired Qualification• Bachelor of Dental Surgery (BDS) from a recognized institution• Valid dental license to practice in IndiaImportant Requirements• Freshers or candidates with up to 1 year of clinical experience• Strong communication and interpersonal skills• Patient-focused approach and empathy• Ability to work in a collaborative team environment• Interest in digital dentistry and modern dental technologiesWhat We Offer• Opportunity to work in a rapidly growing dental health-tech startup• Exposure to advanced dental technologies and digital consultations• Performance-based incentives in addition to base salary• Learning and development opportunities in aligners, implants, and modern dentistryExperience and Skills• 0–1 year of clinical experience• Skills in dental examination and treatment planning• Basic clinical procedures such as scanning, cleaning, and fillings• Patient consultation and communication skills• Ability to maintain accurate clinical recordsCompany OverviewDezy is a rapidly growing dental health-tech company founded in 2019 by IIT and IIM alumni. Backed by investors such as Falcon Edge (Alpha Wave Ventures), Sequoia Capital India, and Chiratae Ventures, the company aims to build one of India and GCC’s most trusted dental care brands. Dezy combines technology and dentistry to provide transparent diagnoses, digital consultations, and high-quality dental treatments.FAQsWhat qualification is required for this role?Candidates must have a BDS degree and a valid dental license to practice in India.Are freshers eligible to apply?Yes, freshers and candidates with up to 1 year of experience can apply.What is the salary offered?The salary ranges from ₹20,000 to ₹25,000 per month along with performance incentives.What dental services does the company specialize in?Dezy specializes in invisible smile aligners, dental implants, smile makeovers, root canal treatments, teeth whitening, dental veneers, and digital dental consultations.Application Tips• Highlight your BDS qualification and internship clinical experience• Mention any exposure to digital dentistry or dental scanning technologies• Emphasize patient communication and teamwork skills• Showcase interest in modern dental treatments like aligners and implants

Why This Role MattersTechnical documentation plays a critical role in ensuring that complex scientific products and solutions are clearly understood and effectively used by customers worldwide. The Technical Writer position at Thermo Fisher Scientific supports the development of accurate, high-quality documentation for advanced bioscience products. By translating technical and scientific concepts into clear instructions, this role helps researchers, laboratories, and organizations operate more efficiently and safely.Working in a globally recognized scientific organization also offers exposure to cutting-edge bioscience innovations and collaborative work with cross-functional teams. This role contributes to improving product usability, maintaining regulatory standards, and supporting scientific advancements that impact healthcare, research, and environmental safety worldwide.Job DescriptionThe Technical Writer I will be responsible for developing, editing, and maintaining comprehensive technical documentation for bioscience products and solutions. This includes creating user guides, manuals, and instructional content that clearly explain complex scientific procedures and technologies.The role requires close collaboration with teams such as research and development, product management, regulatory affairs, and quality assurance to ensure documentation accuracy and completeness. The Technical Writer will also be responsible for maintaining documentation standards, improving existing materials, and managing multiple documentation projects simultaneously.This position demands strong writing skills, attention to detail, and the ability to interpret technical scientific information and convert it into user-friendly content.Key Features of the Role:• Opportunity to work with a leading global life sciences organization• Exposure to cutting-edge bioscience products and technologies• Collaboration with cross-functional teams including R&D and regulatory departments• Opportunity to improve scientific communication and documentation skills• Work on global documentation projects supporting international customers• Career growth opportunities in scientific documentation and technical communicationResponsibilities• Develop, write, and edit technical documents including user manuals, product guides, and technical documentation for bioscience products• Collaborate with subject matter experts, scientists, and product teams to gather technical information• Translate complex scientific data and product details into clear, easy-to-understand documentation• Review and revise existing documentation to improve clarity, accuracy, and usability• Ensure all documents comply with company documentation standards and industry best practices• Manage multiple documentation projects simultaneously while meeting project deadlines• Maintain document repositories, templates, and version control systems• Support continuous improvement of documentation processes and standards• Ensure documentation supports product usability, safety, and regulatory complianceRequired QualificationsEducational Requirements:• Bachelor’s degree in Biosciences, Life Sciences, Biotechnology, Pharmacy, or a related scientific field• Advanced degree in biosciences or related discipline may be preferred• Certification in technical writing or scientific documentation can be an added advantageExperience and Skills:• Experience in technical writing, preferably within the bioscience or life sciences industry• Ability to translate complex scientific information into clear technical documentation• Strong written and verbal communication skills• Excellent attention to detail and documentation accuracy• Familiarity with XML or DITA-based authoring tools such as Oxygen XML Editor or similar platforms• Experience with component content management systems like RWS Tridion Docs or similar tools• Knowledge of Microsoft Office tools including Word, Excel, and PowerPoint• Familiarity with Adobe Creative Suite and other documentation tools• Ability to collaborate effectively with cross-functional teams and subject matter experts• Strong time-management skills and ability to manage multiple projects simultaneously• Willingness to continuously learn new tools, technologies, and documentation standardsSalary Insights:• Entry-level professionals may earn approximately ₹4 LPA – ₹7 LPA• Candidates with relevant experience may earn ₹7 LPA – ₹10 LPA or higher depending on expertise and location• Additional benefits may include health insurance, training programs, and performance incentivesCompany OverviewThermo Fisher Scientific is a global leader in scientific research solutions, laboratory technologies, analytical instruments, and life sciences services. The company supports scientists, researchers, healthcare organizations, and pharmaceutical companies worldwide with innovative products and solutions.With a mission to make the world healthier, cleaner, and safer, Thermo Fisher Scientific provides advanced technologies that accelerate scientific discovery, improve healthcare outcomes, and support environmental sustainability. The company operates globally and collaborates with research institutions and organizations to advance scientific innovation.FAQsWhat does a Technical Writer do in the bioscience industry?A Technical Writer prepares manuals, guides, and product documentation that explain complex scientific products and technologies to end users in a clear and understandable manner.Is prior technical writing experience required?Yes, most organizations prefer candidates with experience in technical writing, especially in life sciences, biotechnology, or bioscience fields.What skills are important for this position?Strong writing skills, scientific knowledge, attention to detail, and the ability to simplify complex technical information are essential for success in this role.What tools are commonly used in technical writing roles?Technical writers often use XML-based authoring tools, documentation management systems, Microsoft Office applications, and graphic editing software.Application Tips• Highlight your technical writing or scientific documentation experience in your resume• Emphasize your educational background in biosciences, biotechnology, or pharmacy• Include examples of documentation, manuals, or writing projects you have worked on• Demonstrate familiarity with documentation tools and content management systems• Showcase your ability to work with scientific teams and translate complex information into simple instructions.

Why This Role MattersClinical trials are essential for evaluating the safety, efficacy, and quality of new medicines before they reach patients. Drug-based clinical trials require strict monitoring, accurate documentation, and compliance with international regulatory guidelines to ensure reliable research outcomes. Monitoring clinical trial sites helps maintain data integrity, participant safety, and regulatory compliance throughout the study lifecycle.The Clinical Research Monitor plays a critical role in supervising clinical trial activities at research sites. This role ensures that clinical trials are conducted according to study protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. By coordinating with investigators, research staff, and sponsors, the monitor ensures that clinical trial processes—from site feasibility to study closeout are performed correctly.At St. John’s Research Institute (SJRI), Bengaluru, the Clinical Research Monitor position supports the TIPS‑3 PHRI Study, a drug-based clinical trial focused on advancing medical research and improving patient outcomes. Professionals in this role contribute significantly to maintaining the quality, safety, and scientific validity of the clinical trial.Job DescriptionThe Clinical Research Monitor will support ongoing clinical trials by coordinating site activities, assisting senior research staff, and monitoring study progress across clinical trial sites. The role includes conducting monitoring visits, providing training to site staff on GCP and study protocols, and ensuring that all trial activities follow regulatory guidelines.The selected candidate will be involved in multiple phases of the clinical trial lifecycle, including site feasibility assessment, initiation visits, participant recruitment monitoring, follow-up phases, and study closeout activities. The role also requires handling audit readiness and supporting inspection processes to ensure compliance with international clinical research standards.Key Features of the Role• Job Title: Clinical Research Monitor (CRM) / Clinical Trial Monitor• Project Type: Drug-Based Clinical Trial• Research Organization: St. John’s Research Institute• Study: TIPS‑3 PHRI Study• Number of Vacancies: 1• Job Location: Bangalore, India• Work Nature: Clinical trial monitoring and site coordination• Travel Requirement: Willingness to travel to clinical trial sitesResponsibilities• Assisting senior researchers in coordinating and monitoring clinical trial activities.• Undergoing training on clinical trial monitoring processes and regulatory requirements.• Scheduling monitoring visits to ensure compliance with study protocols.• Conducting monitoring visits at clinical trial sites to assess study progress.• Providing training to site staff on Good Clinical Practice (GCP) guidelines and study procedures.• Supporting documentation and data verification to maintain study accuracy.• Ensuring clinical trial activities comply with regulatory and ethical standards.• Coordinating with investigators and clinical staff during the recruitment phase of the study.• Monitoring follow-up activities and participant progress throughout the trial.• Supporting study closeout activities and documentation review.Specific Clinical Trial Activities• Site Feasibility Assessment• Site Initiation Visits• Participant Recruitment Phase Monitoring• Follow-Up Phase Coordination• Study Closeout Phase Activities• For-Cause Monitoring Visits• Audit and Regulatory Inspection SupportRequired QualificationsEducational Requirements• MBBS (Bachelor of Medicine and Bachelor of Surgery)• BVSc (Bachelor of Veterinary Science)• BDS (Bachelor of Dental Surgery)• MPHW with Postgraduate Degree• Graduate or Postgraduate degree with a Diploma in Clinical Research• Integrated postgraduate degrees in relevant healthcare or life sciences disciplinesExperience and Skills• Minimum 2 years of experience working as a Site Clinical Research Associate (CRA) or similar clinical research role.• Understanding of clinical trial monitoring and regulatory compliance.• Knowledge of Good Clinical Practice (GCP) guidelines and clinical trial processes.• Ability to coordinate clinical trial site activities effectively.• Strong analytical and documentation skills.• Willingness to travel for site monitoring visits.• Ability to work collaboratively with clinical investigators and research staff.Language RequirementsCandidates should have proficiency in multiple languages, including:• English, Kannada, Hindi, Tamil, Telugu, Other relevant local languagesSalary InsightsThe salary for the Clinical Research Monitor position is competitive and depends on the candidate’s experience and interview performance.Estimated Salary: • ₹50,000 per monthAdditional professional benefits may include:• Hands-on experience in drug-based clinical trials• Exposure to clinical trial monitoring and site management• Opportunities to work with experienced clinical research professionals• Career growth opportunities within clinical research organizationsCompany OverviewSt. John’s Research Institute (SJRI) is a leading biomedical research institution based in Bangalore, India. The institute conducts research in public health, clinical medicine, nutrition, infectious diseases, and chronic disease prevention.SJRI collaborates with national and international research organizations to conduct high-quality clinical trials and health studies. The institute is recognized for its contributions to improving healthcare outcomes through evidence-based research and scientific innovation. Through studies such as the TIPS‑3 PHRI Study, SJRI supports the advancement of clinical research and contributes to global healthcare improvements.FAQs1. What does a Clinical Research Monitor do?A Clinical Research Monitor supervises clinical trial sites to ensure studies follow protocols, regulatory guidelines, and Good Clinical Practice standards.2. What experience is required for this role?Candidates typically need at least two years of experience as a Site Clinical Research Associate (CRA) or in clinical trial monitoring roles.3. Is travel required for this job?Yes, clinical research monitors usually travel to different trial sites to conduct monitoring visits.4. What skills are important for a Clinical Research Monitor?Important skills include clinical trial knowledge, GCP compliance, communication skills, documentation accuracy, and problem-solving ability.5. What career growth opportunities exist after this role?Professionals can advance to roles such as Senior Clinical Research Associate, Clinical Trial Manager, or Clinical Operations Manager.Application Tips• Highlight experience in clinical trial monitoring or site coordination.• Demonstrate knowledge of Good Clinical Practice (GCP) and clinical trial processes.• Mention any experience with site visits, monitoring reports, or audit preparation.• Emphasize communication skills and the ability to coordinate with multiple research teams.• Include certifications or diplomas related to clinical research if applicable.

Why This Role MattersClinical trials require precise financial management to ensure investigators and research sites are compensated accurately and on time. The Investigator Grants Specialist plays a critical role in managing investigator payments, developing site budgets, and ensuring financial transparency across clinical trial operations.By coordinating with project management and clinical operations teams, this role helps maintain smooth financial workflows, ensuring that investigator grants, site budgets, and payment processes comply with contractual agreements and regulatory standards.At Novotech, this role directly contributes to the success of global clinical trials by supporting accurate budgeting, payment tracking, and operational efficiency across multiple research sites.Job DescriptionThe Investigator Grants Specialist supports the project team in managing investigator payments and developing investigator grants using industry-standard systems such as Grant Plan. The role involves close collaboration with project managers, clinical operations teams, and study teams to ensure timely delivery of site budget templates and quarterly site payments.This position requires strong analytical abilities and organizational skills to manage financial aspects of clinical trials, including investigator payment tracking, grant development, and system management within CTMS platforms.All activities must be conducted in accordance with company Standard Operating Procedures (SOPs), client guidelines, and industry regulations to ensure compliance and accuracy in financial processes related to clinical research studies.Key Features of the RoleThis role offers exposure to financial management in clinical research while working with cross-functional teams responsible for trial execution. The position combines financial analysis, system management, and operational coordination to ensure investigator grants and payments are handled efficiently.Professionals in this role gain hands-on experience with CTMS platforms, grant planning systems, and clinical trial budgeting, making it an excellent opportunity for individuals interested in clinical trial operations, finance, and research management.Responsibilities• Review, update and track investigator payments within CTMS systems to ensure accurate records.• Route correspondence appropriately and ensure queries are assigned to the correct team members in a timely manner.• Escalate payment delays or issues when necessary to maintain timely investigator payments.• Review payments against visit data in CTMS to ensure accuracy and compliance with investigator contracts.• Communicate with Project Managers regarding payment inquiries and manage expectations regarding payment timelines.• Support clinical staff in executing accurate and timely investigator payments as per contractual agreements.• Maintain payment schedules for patient visit reimbursements based on sponsor and site contracts.• Process site payments for patient visits and ensure accuracy before submission.• Review site payment reports to ensure accuracy before processing financial transactions.• Prepare investigator payment reports for study status meetings as requested by project managers.• Ensure each assigned study is properly set up and maintained within investigator payment systems.• Analyze and assess Subject Visit Tracking (SVT) requirements based on study complexity.• Create site SVT templates based on Clinical Trial Research Agreements (CTRAs).• Set up master or site-specific SVT templates within CTMS platforms according to project timelines.• Follow company processes and maintain quality standards while performing investigator payment activities.• Participate in clinical operations meetings and contribute to process improvements and SOP development.• Maintain professional communication with external stakeholders including sponsors and research sites.Investigator Grants Activities• Develop investigator grants using industry-standard grant management systems.• Review clinical study protocols and collaborate with project managers to develop accurate investigator budgets.• Deliver investigator grant documents in a timely and accurate manner.• Provide preliminary budget estimates for clients when requested.• Apply industry standards of care when creating budget models for clinical trials.• Address questions related to Fair Market Value (FMV) during budget development.• Communicate with vendors to resolve system-related issues.• Manage and maintain user access lists for relevant systems.• Track finalized investigator budgets and generate reports as required.Required QualificationsEducational RequirementsCandidates must possess a minimum of the following educational qualifications:• Bachelor’s degree in Life Sciences• Degree in Pharmacy or a related healthcare field• Other relevant biomedical or scientific qualifications may also be consideredExperience and Skills• 12–36 months of experience in a Clinical Research Organization (CRO) or similar environment.• Experience in investigator payment processing within clinical trials.• Familiarity with Clinical Trial Management Systems (CTMS) such as Veeva.• Experience working with Grant Plan systems for investigator grant management.• Understanding of Subject Visit Tracking within CTMS platforms.• Strong proficiency in Microsoft Excel and PowerPoint.• Excellent analytical and problem-solving skills.• Strong verbal and written communication skills.• Good negotiation and stakeholder management abilities.• Excellent interpersonal and relationship-building skills.• High level of organization and attention to detail.• Ability to manage multiple tasks while meeting strict deadlines.• Prior experience within pharmaceutical, CRO, or healthcare industries is preferred.Salary Insights• Additional benefits may include performance incentives, health insurance, flexible work arrangements, and professional development programs.Company OverviewNovotech is a global full-service clinical Contract Research Organization (CRO) headquartered in Sydney, Australia. The company provides clinical development services to pharmaceutical and biotechnology companies across Asia-Pacific, North America, and Europe. With over 34 offices worldwide and thousands of site partnerships, Novotech supports clinical trials across all phases of drug development. The organization offers services such as regulatory submissions, data management, statistical analysis, safety monitoring, medical writing, and clinical operations support. Novotech is known for maintaining high quality and security standards, including ISO 27001 certification for information security management and ISO 9001 certification for quality management systems.FAQs1. What does an Investigator Grants Specialist do?An Investigator Grants Specialist manages investigator budgets and payments during clinical trials to ensure sites are compensated accurately and on time.2. What systems are commonly used in this role?Common systems include CTMS platforms such as Veeva, Grant Plan systems, and Microsoft Excel for financial tracking.3. What industries hire for this role?Pharmaceutical companies, biotechnology firms, and Contract Research Organizations (CROs) commonly hire professionals for investigator grants and clinical trial finance roles.4. What career growth opportunities are available?Professionals can progress to roles such as Clinical Trial Budget Manager, Clinical Operations Manager, or Grants & Contracts Manager.Application Tips• Highlight experience in clinical trial payments, investigator grants, or financial operations within CRO environments.• Emphasize familiarity with CTMS platforms such as Veeva and grant management systems.• Demonstrate strong analytical skills and proficiency in Excel for financial tracking.• Showcase communication skills for coordinating with project managers and study teams.• Mention experience in pharmaceutical, CRO, or healthcare industry environments.

Why This Role MattersPharmacovigilance is a critical function in the pharmaceutical and healthcare industry, ensuring patient safety through continuous monitoring of adverse events and compliance with global drug safety regulations. A Drug Safety Associate plays an essential role in maintaining regulatory timelines, processing safety data, and supporting global reporting obligations.This position is ideal for Life Sciences and Pharmacy graduates who want to build a long-term career in pharmacovigilance, regulatory affairs, or drug safety operations. It provides structured exposure to ICSR processing, safety submissions, regulatory intelligence, literature surveillance, and affiliate support activities. Working in a regulated safety environment helps professionals develop strong analytical thinking, documentation accuracy, and compliance discipline—core skills required in global clinical safety operations.Job DescriptionThe Drug Safety Associate will support global pharmacovigilance operations, including Individual Case Safety Report (ICSR) processing, safety submissions, literature monitoring, regulatory support, and affiliate coordination. The role requires adherence to global regulations, client-specific workflows, and internal Standard Operating Procedures (SOPs).The position involves monitoring safety data sources, ensuring accurate data capture in safety databases, maintaining compliance metrics, and supporting regulatory reporting activities. Associates are expected to follow structured workflows, maintain documentation integrity, and escalate issues appropriately.Key Features of the Role:• Exposure to global pharmacovigilance systems• Hands-on ICSR case processing experience• Involvement in regulatory submissions and compliance tracking• Opportunity to work with international health authorities• Learning and development through structured training modules• Participation in audits and inspections• Strong career pathway into senior safety and regulatory rolesResponsibilitiesGeneral Responsibilities• Develop knowledge of safety profiles, labeling, and global regulations• Follow project-specific workflows and procedures• Support compliance with regulatory reporting timelines• Assist in audit and inspection preparation• Review basic safety metrics and escalate issues• Maintain documentation and archiving standards• Participate in LMS training modules and complete assigned coursework• Ensure accurate and timely timesheet submissionICSR Processing• Monitor incoming safety reports from mailboxes, EudraVigilance, and literature sources• Perform literature searches and valid case data entry into safety databases• Triage incoming reports for completeness and validity• Request translations where required• Ensure medical cohesiveness and document consistency• Prepare ADR forms and coversheets• Perform MedDRA coding as per standard guidance• Conduct follow-up and query management• Prepare medically accurate case narratives• Perform quality and validation checks• Support compliance activities and late case investigations• Generate compliance metrics and support reconciliation activities• Perform database updates such as product additions or deletionsSafety Submissions• Submit ICSRs and periodic safety reports to regulatory authorities and ethics committees• Maintain reporting schedules and ensure timely submissions• Perform unblinding for safety reporting when required• Support development of global safety reporting procedures• Register products and organizations for electronic submissions• Track submission compliance and reporting quality• Prepare documentation within EDMS/eTMF systems• Participate in audits and inspections• Coach junior associates when applicableLiterature Search and Review• Develop and maintain search strategies based on client requirements• Screen scientific literature for potential ADRs and safety signals• Perform peer review of literature abstracts• Identify and forward safety signals for medical review• Maintain local journal lists and update search strategies• Insert full-text articles into databases where required• Coordinate with internal and external stakeholders to resolve search-related issuesAffiliate Services• Support communication between global safety teams and local affiliates• Maintain product information systems• Assist with translation and literature monitoring• Support local health authority interactions• Participate in reconciliation activities• Coordinate country-specific literature screeningRegulatory Support and Intelligence• Manage regulatory applications and lifecycle changes• Support global submissions including eCTD registrations and renewals• Track safety reports such as RMP, PBRER, and PASS• Maintain regulatory intelligence databases and trackers• Review country-specific safety reporting requirements• Collaborate with global pharmacovigilance intelligence teams• Ensure compliance with Service Level Agreements and KPIsRequired QualificationsCandidates must demonstrate foundational knowledge of pharmacovigilance processes and regulatory frameworks. Strong attention to detail, analytical ability, and documentation accuracy are essential. The role requires comfort working with structured databases and adherence to compliance-driven workflows.Educational Requirements:• Degree in Life Sciences, Health Sciences, or Biomedical Sciences• Pharmacy, Microbiology, Biochemistry, Biotechnology, or related disciplines preferred• Equivalent relevant qualification or work experience may be consideredExperience and Skills:• Foundational knowledge of drug safety regulations• Basic understanding of healthcare terminology• Familiarity with ICH guidelines and regional requirements (preferred)• Introductory exposure to pharmacovigilance databases• Basic proficiency in MS Office applications• Good communication and organizational skills• Strong willingness to learn and grow in drug safety operationsSalary InsightsCompensation is aligned with entry-level to junior pharmacovigilance roles in the healthcare industry. Salary may vary depending on experience, region, and organizational banding structure. Employees typically receive structured training, compliance exposure, and long-term growth opportunities within drug safety and regulatory domains.Company OverviewThe hiring organization operates within global pharmacovigilance and regulatory compliance frameworks, supporting sponsors and healthcare clients worldwide. The company maintains strict adherence to international drug safety standards, regulatory timelines, and quality benchmarks. Employees benefit from structured learning environments, exposure to global safety operations, and professional growth within clinical safety and regulatory affairs functions.FAQsIs prior pharmacovigilance experience mandatory?No, related healthcare experience is advantageous but not mandatory.What databases are commonly used in this role?Safety databases for ICSR processing and regulatory submission portals.Is this role suitable for fresh graduates?Yes, candidates with foundational knowledge and strong learning intent can apply.Does the role involve regulatory submissions?Yes, safety submissions to health authorities are a core responsibility.What career growth can be expected?Progression into Senior Drug Safety Associate, Safety Reporting Specialist, Regulatory Specialist, or PV Quality roles.Application Tips• Revise ICH-GCP and pharmacovigilance basics• Understand ICSR workflow and MedDRA coding fundamentals• Highlight internship or safety database exposure• Demonstrate attention to detail during interviews• Emphasize willingness to learn global safety regulations

Why This Role MattersThe Investigator Support Assistant plays a vital role in ensuring smooth coordination between global clinical research teams and investigator sites. In clinical trials, timely communication, documentation accuracy, and compliance with regulatory standards directly impact patient safety and study success. This position supports Global Investigator Support (GIS) functions by managing site communication, resolving operational queries, and coordinating documentation and logistics processes. By ensuring patient safety remains the top operational priority and maintaining workflow efficiency, this role contributes significantly to high-quality clinical trial execution and global regulatory compliance.Job DescriptionThe Investigator Support Assistant supports global clinical research operations by assisting investigator sites, coordinating documentation, managing logistics processes, and resolving workflow-related issues. The role involves regular communication with investigator sites, tracking documentation, supporting portal access, handling shipping coordination, and ensuring adherence to Standard Operating Procedures (SOPs). This position is ideal for life sciences and pharmacy graduates seeking entry-level opportunities in clinical research operations, global investigator services, and site management within a multinational CRO environment.Key Features of the Role:• Direct exposure to global clinical trial workflows• Interaction with international investigator sites• Hands-on experience in site support and logistics coordination• Opportunity to work within a compliance-driven environment• Structured training and career development programs• Entry-level opportunity in clinical research operations• Strong foundation for future roles in clinical operations and pharmacovigilanceResponsibilities• Communicate with investigator sites through email and assigned communication platforms• Escalate patient safety concerns promptly to appropriate teams• Assist investigator sites with portal login access and system-related queries• Notify sites regarding specimen pending arrival reports• Compile and distribute communication related to new policies and procedural updates• Prepare airway bills and shipping documentation for site logistics• Coordinate with internal departments to resolve delivery errors• Maintain and update investigator database records• Investigate and resolve simple to moderate system hold issues• Respond to project-related queries within defined timelines• Escalate unresolved concerns to assigned global coordinators• Document service issues and ensure proper resolution• Review and comply with Standard Operating Procedures (SOPs)• Maintain training documentation and compliance records• Track workflow metrics and ensure timely reporting• Participate in onboarding and mandatory corporate training• Attend departmental meetings and continuous learning sessions• Support administrative tasks related to global investigator coordinationRequired QualificationsCandidates should possess an academic background in Life Sciences, Pharmacy, Biotechnology, Microbiology, Clinical Research, or related disciplines. Fresh graduates with strong communication skills and an interest in clinical research operations are encouraged to apply. Candidates with up to two years of experience in clinical operations or site coordination may also be considered.Educational Requirements:• B.Pharm or M.Pharm• B.Sc or M.Sc in Life Sciences, Biotechnology, Microbiology, or related fields• Clinical Research graduates• Equivalent qualifications in health sciences or allied disciplinesExperience and Skills:• 0–2 years of experience in clinical research or healthcare operations• Strong written and verbal communication skills• Basic understanding of clinical trial processes and workflows• Ability to manage documentation accurately and efficiently• Proficiency in MS Office applications• Ability to prioritize tasks and manage multiple responsibilities• Strong attention to detail and compliance awareness• Good problem-solving and query-handling skills• Team-oriented mindset with the ability to work in a global environment• Professional communication skills suitable for international coordinationSalary InsightsThe estimated salary range for this position in the Bangalore market is approximately ₹3,00,000 to ₹4,80,000 per annum (CTC), depending on qualifications, communication skills, and prior experience. In addition to base compensation, employees may receive structured training, performance-based growth opportunities, and exposure to global clinical operations processes.Company OverviewThe hiring organization is a globally recognized life sciences company providing comprehensive drug development, laboratory, and clinical research services. With operations across multiple countries, the organization supports pharmaceutical and biotechnology companies in conducting safe, efficient, and compliant clinical trials. The company emphasizes diversity, inclusion, regulatory excellence, and professional development, offering employees a dynamic environment for long-term career growth in clinical research and healthcare services.FAQsQ1. Is this role suitable for freshers?Yes, fresh graduates with strong communication skills and an interest in clinical research are eligible to apply.Q2. Is prior clinical research experience mandatory?No, prior experience is not mandatory, but basic knowledge of clinical trial processes is beneficial.Q3. What kind of exposure does this role provide?The role offers exposure to global investigator coordination, logistics management, documentation workflows, and compliance-driven operations.Q4. What career growth opportunities are available?Employees may progress to roles such as Clinical Operations Coordinator, Project Support Associate, Site Management Associate, or Pharmacovigilance Associate.Q5. Is this an office-based role?The role is typically office-based in Bangalore, depending on organizational policies.Application Tips• Highlight communication skills and documentation accuracy in your resume• Mention any academic projects or internships related to clinical research• Demonstrate understanding of SOP compliance and workflow management• Showcase proficiency in MS Office and database handling• Prepare examples of multitasking and problem-solving during interviews• Emphasize willingness to learn and adapt to global processes

Why This Role MattersClinical research projects require strong coordination, structured planning, and efficient documentation to ensure successful execution within timelines and regulatory frameworks. A Project Associate plays a critical support role in maintaining operational efficiency, communication flow, and compliance across clinical development programs.At ICON plc, a globally recognized healthcare intelligence and clinical research organization, this position contributes directly to shaping the future of clinical development. The role supports project managers and clinical operations teams, ensuring that administrative and operational activities are executed accurately and on time. For professionals with 1–3 years of experience in Project Management and Clinical Operations, this opportunity provides structured growth within a global CRO environment.Job DescriptionICON plc is seeking a Project Associate with 1 to 3 years of experience in Project Management and Clinical Operations (ClinOps), along with working knowledge of CTMS and eTMF systems. The selected candidate will assist in planning, coordinating, and supporting clinical projects to ensure smooth operational delivery.The role involves administrative oversight, cross-functional collaboration, documentation management, and stakeholder communication. Candidates must demonstrate strong organizational skills, attention to detail, and the ability to manage multiple responsibilities in a dynamic environment.Key Features of the Role:• Exposure to global clinical research projects• Involvement in CTMS and eTMF systems• Hands-on project coordination experience• Opportunity to work within a leading CRO environment• Career progression in clinical project management• Participation in strategic planning discussionsResponsibilities• Support the development and execution of project plans• Coordinate project activities including meeting scheduling and documentation• Prepare agendas, record minutes, and maintain action trackers• Collaborate with cross-functional teams to ensure smooth communication• Contribute to project documentation and reporting for stakeholders• Provide guidance to junior associates when required• Maintain transparency and integrity in project support processes• Participate in project planning and decision-making discussions• Stay updated on industry trends and best practicesRequired QualificationsCandidates should demonstrate foundational project management knowledge and clinical operations exposure. Familiarity with CTMS and eTMF systems is essential. Strong organizational discipline and communication skills are critical to succeed in this role.Educational Requirements:• Bachelor’s or Master’s degree in Allied Health Sciences or Life Sciences disciplineExperience and Skills:• 1 to 3 years of experience in Project Management and Clinical Operations• Working knowledge of CTMS and eTMF systems• Excellent organizational and multitasking abilities• Strong written and verbal communication skills (Fluency in English required)• Detail-oriented mindset with problem-solving capabilities• Ability to manage deadlines in fast-paced environments• Collaborative team player with professional conductSalary InsightsCompensation is competitive and aligned with global CRO standards. Salary varies based on experience, expertise, and internal banding. In addition to base pay, ICON offers comprehensive benefits focused on employee well-being and work-life balance.Company OverviewICON plc is a world-leading clinical research organization specializing in healthcare intelligence and clinical development solutions. The company partners with pharmaceutical, biotechnology, and medical device organizations to accelerate innovation and improve patient outcomes.ICON is known for its inclusive work culture, strong performance-driven environment, and structured career development opportunities. Employees benefit from global exposure, collaborative teamwork, and access to industry-leading clinical technologies.FAQsIs CTMS and eTMF knowledge mandatory?Yes, working knowledge of CTMS and eTMF systems is required.What level of experience is needed?Candidates must have 1 to 3 years of experience in Project Management and Clinical Operations.Is this role client-facing?The role involves stakeholder coordination and cross-functional collaboration but primarily supports internal project teams.What growth opportunities are available?Career progression may include Senior Project Associate, Project Specialist, Clinical Project Coordinator, or Project Manager roles.Does ICON offer additional benefits?Yes, including health insurance, retirement planning, employee assistance programs, and flexible benefits.Application Tips• Highlight CTMS and eTMF system experience clearly on your resume• Showcase examples of project coordination and documentation management• Demonstrate strong communication and multitasking skills• Prepare to discuss your role in previous clinical projects• Emphasize ability to work within global cross-functional teams

Why This Role MattersThe Investigator Grants Specialist plays a critical role in ensuring the financial accuracy, transparency, and efficiency of clinical trial operations. In clinical research, timely and accurate investigator payments are essential for maintaining strong site relationships, ensuring compliance with contractual agreements, and supporting uninterrupted study progress. This role directly contributes to operational excellence by managing site budgets, processing investigator payments, and supporting grant development activities.By ensuring payments are aligned with subject visits, contractual terms, and study timelines, the Investigator Grants Specialist helps safeguard the integrity of clinical trials. The position also supports financial planning and budget development using industry-standard systems, ensuring fair market value compliance and regulatory alignment. Ultimately, this role strengthens partnerships between sponsors, research sites, and internal teams while contributing to the successful execution of clinical programs.Job DescriptionThe Investigator Grants Specialist is responsible for managing investigator payment processes and developing investigator grants using standardized systems such as Grant Plan and CTMS platforms. The role works closely with Project Management and Clinical Operations teams to ensure accurate site budget templates, subject visit tracking (SVT) setup, and timely processing of quarterly site payments.All activities are performed in compliance with company SOPs, client guidelines, and regulatory standards. The specialist ensures high-quality financial data management, timely escalation of issues, and strong communication across cross-functional teams. The role requires strong analytical capabilities, attention to detail, and the ability to manage multiple studies simultaneously.Key Features of the Role:• Management of investigator payments aligned with subject visit data.• Development and maintenance of investigator grants using industry-standard tools.• Close collaboration with Clinical Operations and Project Management teams.• Exposure to complex, multi-country clinical projects.• Involvement in budget modeling and fair market value assessment.• Responsibility for maintaining compliance with financial and regulatory requirements.• Participation in process improvement and SOP development initiatives.Responsibilities• Review, update, and track all investigator payments accurately within CTMS.• Ensure payments are processed in accordance with investigator contracts and agreed schedules.• Escalate payment discrepancies or delays to appropriate stakeholders.• Coordinate with Project Managers to resolve payment-related queries efficiently.• Review visit data in CTMS to ensure accurate subject visit tracking before payment release.• Prepare investigator payment reports for study meetings and internal reviews.• Maintain accurate setup and management of Subject Visit Tracking (SVT) templates.• Create site-specific SVTs based on Clinical Trial Research Agreements (CTRAs).• Ensure master and site-specific templates are built accurately within required timelines.• Develop investigator grants using Grant Plan or equivalent systems.• Review study protocols to prepare accurate and complete budget models.• Provide initial budget estimates for sponsors and support complex project assignments.• Apply industry-standard cost benchmarks and fair market value principles.• Coordinate with vendors for system access and technical support.• Track finalized budgets and maintain organized documentation for audits.• Participate in departmental meetings and contribute to process enhancement initiatives.• Maintain professional communication with sponsors, sites, and external stakeholders.Required Qualifications• Strong understanding of clinical trial payment processes.• Knowledge of CTMS platforms such as Veeva.• Experience in investigator grant development and budget preparation.• High level of attention to detail and organizational skills.• Strong analytical and problem-solving capabilities.• Ability to manage multiple tasks and meet strict deadlines.• Excellent written and verbal communication skills.Educational Requirements:• Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or a related field is mandatory.• Advanced certifications in clinical research or finance are an added advantage.Experience and Skills:• 12–36 months of experience in a Clinical Research Organization (CRO), pharmaceutical, or healthcare environment.• Experience working in investigator payment processing.• Hands-on experience with CTMS and Grant Plan systems.• Strong proficiency in MS Excel and PowerPoint.• Understanding of Subject Visit Tracking and contract-based payment models.• Strong interpersonal and relationship-building skills.• Ability to work independently while collaborating within cross-functional teams.Salary InsightsThe salary for an Investigator Grants Specialist varies depending on experience, technical expertise, and project complexity. Candidates with hands-on CTMS and grant development experience typically command competitive compensation within the clinical research industry. Additional benefits may include performance-based incentives, flexible working arrangements, health benefits, paid parental leave, wellness programs, and professional development opportunities.Company OverviewNovotech is a global full-service Clinical Contract Research Organization (CRO) headquartered in Sydney, Australia. With offices across Asia-Pacific, North America, and Europe, the organization supports clinical development services across all phases and therapeutic areas. Novotech provides feasibility assessments, regulatory submissions, safety solutions, statistical analysis, medical monitoring, and project management services.The company maintains internationally recognized certifications including ISO 9001 for Quality Management and ISO 27001 for Information Security Management Systems. Novotech is committed to fostering an inclusive workplace, promoting diversity, and maintaining high professional standards across global operations.FAQs1. Is prior CRO experience mandatory?Yes, prior experience in a CRO, pharmaceutical, or healthcare setting is preferred.2. Is experience in CTMS essential?Yes, practical experience in CTMS systems such as Veeva is important for managing payments and tracking subject visits.3. Will the role involve handling complex budgets?Yes, candidates may be assigned to complex projects requiring advanced budget modeling and fair market value assessment.4. Does this role involve cross-functional collaboration?Yes, the position requires regular interaction with Project Managers, Clinical Operations teams, sponsors, and research sites.Application Tips• Highlight your CTMS and investigator payment experience clearly in your resume.• Emphasize any grant development or budget modeling exposure.• Showcase proficiency in MS Excel, especially financial tracking and reporting.• Demonstrate examples of managing multiple studies or tight deadlines.• Mention experience handling sponsor or site communication professionally.

Why This Role MattersThe Specialist I, Global Clinical Solutions role at AstraZeneca plays a critical part in ensuring clinical trials run efficiently, accurately, and in compliance with global standards. Behind every successful clinical study is a strong foundation of clean data, reliable systems, and precise clinical coding. This position safeguards that foundation.By supporting study delivery systems, maintaining coding accuracy, and providing first-line user support, you directly contribute to faster decision-making and smoother trial execution. The impact of this role extends beyond data—it helps accelerate the development of life-changing medicines for patients worldwide.Job DescriptionThe Specialist, Global Clinical Solutions will support global study teams by maintaining key clinical systems, ensuring data integrity, performing clinical coding activities, and resolving system-related queries. The role combines technical expertise, operational coordination, and user support to ensure global trials operate seamlessly.The candidate will collaborate across Clinical Development, Data Management, and Operations teams while contributing to process improvements and system integration initiatives.Key Features of the Role:• Global clinical trial exposure• Hands-on clinical coding and system stewardship• Cross-functional collaboration with study teams• First-line system and user support responsibilities• Hybrid work model (minimum three days per week in office)• Opportunity to contribute to non-drug project proposalsResponsibilities• Maintain systems related to Financial Disclosure, Drug Return and Destruction, Pairs Investigator Database, Investigator Safety Letter Distribution, and Clinical Trial Registration• Provide first-line user support for study delivery systems and resolve issues promptly• Monitor and maintain data integrity within Study Delivery (SD) systems• Process financial charges associated with study delivery support activities• Perform accurate clinical coding or review CRO-coded data (medical history, surgical history, adverse events, drugs) using approved coding dictionaries• Raise, track, and resolve coding-related queries according to global and local study processes• Monitor and respond to coding-related GDMRs and escalate to the GCDMT when required• Contribute to development of cases prioritizing non-drug project proposals• Share knowledge, maintain communication tools, and support global system integration• Ensure compliance with Safety, Health, and Environment (SHE) standardsEducational Requirements:• Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, or a related fieldEssential Skills and Experience:• Experience maintaining clinical study delivery systems• Strong understanding of clinical coding practices and dictionaries (e.g., MedDRA, WHO Drug)• Hands-on experience coding clinical study data• Knowledge of global and local study processes and timelines• Experience in first-line user support and data integrity monitoring• Familiarity with financial processing related to study support activities• Strong attention to detail and analytical skills• Effective communication and collaboration abilitiesDesirable Skills and Experience:• Experience supporting non-drug project proposal prioritization• Exposure to global system integration initiatives• Ability to contribute to continuous improvement strategies• Leadership mindset with collaborative approach• Commitment to quality, compliance, and innovationImportant Date• Closing Date: 03-Apr-2026Company OverviewAstraZeneca is a global, science-led biopharmaceutical company focused on the discovery, development, and commercialization of prescription medicines. The organization emphasizes innovation, digital transformation, and collaborative science to accelerate drug development and improve patient outcomes worldwide.With strong investments in data science, AI capabilities, and global collaboration, AstraZeneca fosters a culture of inclusion, scientific curiosity, and operational excellence.Work ModelThe role follows a hybrid working model with an average expectation of a minimum of three days per week in the office, balancing collaboration with individual flexibility.FAQs1. What type of role is this?It is a global clinical operations and systems support role focused on clinical coding and study delivery systems.2. Is clinical coding experience mandatory?Yes, hands-on coding or review experience of clinical study data is essential.3. Where is the job location?The position is based in Bangalore, India.4. What is the last date to apply?The closing date is 03-Apr-2026.5. Does the role involve cross-functional collaboration?Yes, the role requires working closely with Clinical Development, Data Management, and Operations teams globally.Application Tips• Highlight experience in clinical coding and study systems• Mention familiarity with coding dictionaries such as MedDRA and WHO Drug• Demonstrate experience in resolving system queries and supporting users• Showcase cross-functional collaboration examples• Apply early to ensure timely consideration