Clinical Research Jobs in Kolkata
Browse the latest opportunities in Clinical Research Kolkata.
Clinical Research Quality Control (QC) Officer
Why This Role MattersClinical trials are essential for developing new medicines, vaccines, and medical treatments. However, the success of these trials depends not only on data collection but also on the accuracy, integrity, and regulatory compliance of the data generated during the research process. This is where Clinical Research Quality Control (QC) Officers play a critical role.Quality Control professionals in clinical research ensure that every stage of a clinical trial follows strict regulatory standards such as International Council for Harmonisation – Good Clinical Practice (ICH-GCP). Their work ensures that clinical trial data is reliable, accurate, and ethically obtained, which ultimately protects patient safety and ensures that research findings are credible.QC Officers act as internal reviewers who verify clinical trial documentation, study records, and regulatory files before they are submitted for audits or regulatory inspections. Their role helps identify errors, inconsistencies, or protocol deviations early in the research process so corrective actions can be implemented promptly.In the clinical research ecosystem, maintaining high-quality data is essential for regulatory approvals and drug development. Without effective quality control processes, clinical trial outcomes may be questioned, which could delay new treatments from reaching patients. Therefore, QC professionals serve as an important safeguard for both research quality and patient safety.For professionals with a background in life sciences, pharmacy, or biotechnology, the role of a Clinical Research QC Officer provides an excellent opportunity to build expertise in regulatory compliance, documentation review, and clinical trial quality assurance.Job DescriptionA leading Clinical Research Organization is hiring a Quality Control (QC) Officer in Kolkata, West Bengal, to support clinical trial quality management and regulatory compliance activities.In this role, the QC Officer will be responsible for reviewing clinical trial documentation, verifying protocol compliance, and ensuring that all clinical research activities align with regulatory standards and Good Clinical Practice guidelines. The position focuses heavily on reviewing study records, verifying data accuracy, and ensuring that clinical documentation meets regulatory expectations. The QC Officer will also support internal quality checks prior to monitoring visits, regulatory audits, and inspections. This includes reviewing essential study documents such as Trial Master Files (TMF), Site Master Files (SMF), and informed consent documentation.Another important responsibility involves collaborating with study teams to identify and resolve discrepancies in clinical trial data. The QC Officer may participate in Root Cause Analysis (RCA) and assist in implementing Corrective and Preventive Actions (CAPA) to address quality issues. Professionals in this role will work closely with clinical research associates, data managers, investigators, and regulatory teams to ensure that clinical trials are conducted according to approved protocols and regulatory guidelines. This role offers valuable experience for professionals who wish to build long-term careers in Clinical Research Quality Assurance, regulatory compliance, and clinical trial management.Key Features of the Role:• Opportunity to work in clinical research quality control and regulatory compliance• Hands-on experience reviewing clinical trial documentation and study records• Exposure to Trial Master File (TMF) and Site Master File (SMF) management• Involvement in CAPA implementation and Root Cause Analysis• Experience preparing clinical trials for regulatory audits and inspections• Career growth opportunities in Clinical Research Quality AssuranceResponsibilities• Perform quality control review of clinical trial documents and source data.• Verify accuracy of data recorded in electronic Case Report Forms (eCRFs).• Ensure compliance with clinical trial protocols and regulatory guidelines.• Review Trial Master File (TMF) and Site Master File (SMF) documentation.• Verify informed consent documentation and regulatory approvals.• Monitor Investigational Product (IP) accountability and storage records.• Conduct internal quality checks prior to monitoring visits or audits.• Identify discrepancies in clinical trial documentation and data records.• Collaborate with study teams to resolve data inconsistencies.• Support Root Cause Analysis (RCA) investigations for quality issues.• Assist in implementing Corrective and Preventive Actions (CAPA).• Maintain documentation required for regulatory inspections and audits.Required Qualifications• Strong knowledge of clinical trial processes and quality control procedures• Understanding of regulatory guidelines including ICH-GCP• Excellent documentation review and analytical abilities• High attention to detail for identifying discrepancies in clinical records• Ability to collaborate effectively with cross-functional clinical research teamsEducational Requirements:• Bachelor’s degree in Life Sciences• Bachelor’s degree in Pharmacy (B.Pharm)• Degree in Biotechnology or related biomedical fieldExperience and Skills:• Experience in clinical trials, site operations, or quality control activities• Familiarity with clinical research documentation and regulatory records• Strong understanding of ICH-GCP guidelines and compliance standards• Experience reviewing clinical trial data and documentation• Ability to perform data verification and documentation quality checks• Knowledge of Root Cause Analysis and CAPA implementation processes• Strong analytical thinking and problem-solving abilities• Effective communication and teamwork skillsSalary InsightsThe estimated salary for Clinical Research QC Officer roles in India typically ranges between ₹3,00,000 and ₹5,50,000 per year, depending on the candidate’s experience, technical skills, and familiarity with clinical research regulations. Additional benefits may include exposure to regulatory audits, professional training in quality assurance processes, and opportunities for advancement within the clinical research industry.Company OverviewClinical Research Organizations (CROs) play an essential role in supporting pharmaceutical companies, biotechnology firms, and medical research institutions in conducting clinical trials. These organizations provide services such as clinical trial monitoring, data management, regulatory support, and quality assurance. By joining a CRO in a quality control role, professionals gain exposure to global clinical research standards and regulatory frameworks. This experience is valuable for building careers in clinical research quality assurance, regulatory affairs, and clinical operations management. Working in the CRO environment also provides opportunities to collaborate with international sponsors, clinical investigators, and healthcare professionals involved in drug development and clinical research.FAQs1. What does a Clinical Research QC Officer do?A QC Officer reviews clinical trial documentation, verifies data accuracy, ensures regulatory compliance, and helps maintain the overall quality of clinical research activities.2. What is the difference between QC and QA in clinical research?Quality Control focuses on reviewing and verifying data and documentation, while Quality Assurance focuses on overall systems, processes, and compliance frameworks.3. Is certification in clinical research required?Certification is not always mandatory but can improve job prospects and demonstrate knowledge of clinical trial processes.4. What career growth opportunities are available after this role?Professionals can progress to Clinical QA Specialist, Senior Quality Auditor, Regulatory Affairs Specialist, or Clinical Project Manager roles.Application Tips• Highlight your knowledge of ICH-GCP guidelines and regulatory compliance.• Include experience related to TMF, SMF, and clinical trial documentation review.• Mention any clinical research certification or training programs.• Showcase your attention to detail and analytical skills.• Emphasize experience with CAPA implementation or Root Cause Analysis.• Ensure your resume reflects experience with clinical trial data verification and quality control processes.
Clinical Data Coder
Why This Role MattersClinical research studies generate massive volumes of medical data including patient records, adverse events, medication history, laboratory results, and treatment outcomes. In order for this data to be useful for regulatory submissions, safety monitoring, and scientific analysis, it must be accurately reviewed, standardized, and coded using internationally recognized medical dictionaries.The role of a Clinical Data Coder is essential in transforming raw clinical data into structured and standardized information that can be used for clinical analysis and regulatory reporting. By applying medical coding standards such as MedDRA and WHODD, professionals in this role help ensure that adverse events, medications, and medical histories are categorized consistently across clinical trials.This role supports the entire clinical data lifecycle, from study startup to database lock. Accurate coding allows researchers, statisticians, and regulatory authorities to identify trends, evaluate treatment safety, and make evidence-based decisions during drug development.Professionals working in this role collaborate closely with data management teams, safety teams, clinical research associates, and project managers. Their work directly contributes to maintaining the quality and integrity of clinical trial databases while ensuring compliance with regulatory standards and industry best practices.Job DescriptionThe Clinical Data Coder is responsible for performing clinical data management and medical coding activities that support the successful execution of clinical trials. This role requires reviewing clinical datasets, coding medical terms using standardized dictionaries, validating coding systems, and resolving data queries to maintain data accuracy.The candidate will work within the Data Management team to ensure that coding activities are delivered efficiently while meeting sponsor expectations and regulatory standards. The role may involve serving as a Clinical Data Coder, Lead Coder, or Data Operations Coordinator (DOC) depending on the project requirements.Responsibilities also include supporting coding-related activities across the full clinical study lifecycle, performing quality control procedures, testing coding applications, and assisting with reconciliation of serious adverse events. The role requires strong analytical skills, excellent attention to detail, and a solid understanding of clinical data management processes.The candidate will also collaborate with cross-functional teams, maintain documentation, and ensure that all coding activities comply with company operating procedures and regulatory guidelines.Key Features of the Role:• Exposure to global clinical trial data management processes• Hands-on experience with medical coding dictionaries such as MedDRA and WHODD• Opportunity to work on multiple clinical trial protocols• Involvement in Serious Adverse Event reconciliation activities• Experience with coding validation and quality control procedures• Collaboration with global clinical research teams• Opportunities to take leadership responsibilities in coding projectsResponsibilities• Serve independently as a Clinical Data Coder, Lead Coder, or Data Operations Coordinator for assigned protocols.• Manage delivery of coding activities and standalone coding projects throughout the study lifecycle.• Validate and test coding applications and programming of coding reports.• Test coding-related datasets, edits, and programming activities when required.• Perform data management and coding-related tasks including clinical data review and query resolution.• Write and resolve data clarification queries to ensure data consistency.• Manage coding timelines with guidance from the Data Operations Coordinator or Data Team Lead.• Perform Serious Adverse Event reconciliation activities.• Act as a backup for Lead Coder, Data Operations Coordinator, or Data Team Lead when required.• Conduct quality control checks to ensure high coding accuracy and data integrity.• Assist in implementing new technologies and improvements in coding processes.• Provide coding-related solutions and recommendations to the data management team.• Handle audit requirements for assigned clinical studies and coding projects.• Follow company standard operating procedures and work instructions.• Perform additional tasks assigned by the study team or management.• Maintain strong communication and collaborative working relationships within the team.Required Qualifications• Strong understanding of clinical data management and medical coding processes• Excellent analytical and problem-solving skills• Strong attention to detail when reviewing clinical data• Ability to work independently and manage multiple tasks simultaneously• Strong written and verbal communication skills• Ability to collaborate effectively with cross-functional teamsEducational Requirements:• Bachelor’s degree in Pharmacy, Medicine, Dentistry, Nursing, Life Sciences, or a related healthcare field• Equivalent educational background with relevant training may also be considered• Knowledge of pharmacology, anatomy, and physiology is advantageousExperience and Skills:• Minimum 2 years of experience in clinical data management or medical coding• Strong knowledge of medical terminologies used in clinical research• Experience with medical coding dictionaries such as MedDRA and WHODD• Understanding of the clinical data management lifecycle from study startup to database lock• Familiarity with clinical databases and coding applications• Experience performing data review, query resolution, and reconciliation processes• Knowledge of database technologies related to clinical data management• Strong organizational and leadership abilitiesSalary InsightsClinical Data Coders and Clinical Data Management professionals receive competitive compensation depending on their experience and technical expertise. In addition to salary, employees may receive benefits such as health insurance, performance bonuses, training programs, and opportunities to work on international clinical trials. With experience, professionals can progress to roles such as Senior Clinical Data Coder, Clinical Data Manager, Data Team Lead, or Clinical Project Manager.Company OverviewIQVIA is a global leader in clinical research services, healthcare analytics, and commercial insights for the life sciences and healthcare industries. The company provides advanced data solutions, clinical trial management services, and healthcare intelligence to pharmaceutical, biotechnology, and medical device organizations worldwide.Operating in more than 100 countries, IQVIA combines cutting-edge technology, deep scientific expertise, and extensive healthcare data to accelerate the development and commercialization of innovative medical treatments. The organization supports the full lifecycle of healthcare product development, from clinical trials and regulatory submissions to real-world evidence generation.IQVIA is committed to maintaining the highest standards of integrity, quality, and innovation while helping improve patient outcomes and population health globally.FAQs1. What does a Clinical Data Coder do?A Clinical Data Coder reviews clinical trial data and converts medical terms into standardized codes using dictionaries like MedDRA and WHODD.2. What skills are important for this role?Knowledge of medical terminology, attention to detail, analytical skills, and understanding of clinical data management processes are essential.3. Is clinical research experience required?Yes, most roles require at least two years of experience in clinical data management or medical coding.4. What are the career growth opportunities?Professionals can advance to Senior Data Coder, Clinical Data Manager, Data Team Lead, or Clinical Project Manager roles.Application Tips• Highlight your knowledge of medical terminology, pharmacology, anatomy, and physiology in your resume.• Clearly mention experience with medical coding dictionaries such as MedDRA and WHODD.• Include your experience in clinical data review, query resolution, and data reconciliation.• Emphasize familiarity with clinical databases and data management systems.• Demonstrate your attention to detail and ability to manage clinical datasets accurately.• Mention any experience working in clinical research teams or global study environments.• Keep your resume structured and highlight clinical data management skills relevant to the role.
Clinical Research Associate (CRA)
Roles & Responsibilities• Conduct Site Selection Visits (SSV), Site Initiation Visits (SIV), Interim Monitoring Visits (IMV), and Close-Out Visits (COV)• Ensure clinical trials are conducted in compliance with ICH-GCP guidelines, SOPs, and applicable regulatory requirements• Monitor study progress to ensure adherence to approved protocol, timelines, and quality standards• Perform Source Data Verification (SDV) and validate CRF/eCRF entries for accuracy and completeness• Identify, document, and follow up on protocol deviations, discrepancies, and corrective actions• Maintain, review, and update Trial Master File (TMF) documentation• Ensure proper informed consent process compliance and documentation• Coordinate with investigators, site staff, CROs, and sponsors for smooth study execution• Track, review, and report Serious Adverse Events (SAEs) as per regulatory timelines• Prepare detailed monitoring visit reports and follow-up letters• Support audit and inspection readiness by ensuring documentation accuracy and completeness• Assist in regulatory submissions and essential document managementQualification• B.Pharm (Bachelor of Pharmacy) / M.Pharm (Master of Pharmacy)• BSc / MSc in Life Sciences, Clinical Research, or related disciplineExperience• 1–2 years of hands-on experience in clinical trial monitoring• Working knowledge of ICH-GCP guidelines• Experience in TMF maintenance and SAE reportingSkills• Strong clinical trial monitoring expertise• Proficiency in Source Data Verification (SDV)• Experience with eCRF documentation and review• Strong understanding of regulatory compliance frameworks• Excellent documentation and reporting skills• Strong communication and site coordination abilities• Ability to manage multiple study activities efficiently• High attention to detail and quality-focused approachAbout the OrganizationDesun Hospital is a multi-specialty healthcare institution in Kolkata with a structured clinical research environment. The hospital provides opportunities for clinical research professionals to gain hands-on experience in monitoring, regulatory compliance, and investigator coordination within a hospital-based research setup.
Clinical Trial Coordinator
Why This Role MattersClinical trials are essential for advancing medical science and improving patient outcomes by evaluating the safety and effectiveness of new treatments. Clinical Trial Coordinators ensure that research studies are conducted efficiently, ethically, and in compliance with regulatory standards. The Trial Coordinator position at Tata Memorial Centre offers an opportunity to support clinical research activities at a leading oncology research institution. Professionals in this role assist investigators in managing study documentation, coordinating research activities, and ensuring adherence to clinical trial protocols.Working within a specialized oncology research environment at Homi Bhabha Cancer Hospital & Research Centre, the Trial Coordinator will contribute to the execution of clinical research studies aimed at improving cancer treatment and patient care. For candidates with a background in life sciences and clinical research training, this role offers a strong foundation for building a career in clinical trials, research coordination, and healthcare research operations.Job DescriptionTata Memorial Centre is conducting a walk-in interview to recruit a Trial Coordinator for clinical research activities at Homi Bhabha Cancer Hospital & Research Centre. The selected candidate will support clinical research studies by assisting investigators with study coordination, documentation management, and research data handling. The role involves coordinating clinical trial activities, maintaining research records, and ensuring that study procedures follow regulatory guidelines and institutional protocols. This is a contractual position with an initial tenure of six months, which may be extended based on project requirements and institutional needs.Key Features of the Role• Opportunity to work in clinical research within a leading oncology institution• Exposure to clinical trial coordination and research documentation• Involvement in patient data management and study monitoring activities• Participation in maintaining compliance with clinical research regulations• Opportunity to gain experience in cancer research and clinical trialsResponsibilitiesClinical Trial CoordinationAssist investigators and research teams in coordinating clinical trial activities. Support the execution of clinical research protocols while ensuring adherence to institutional and regulatory guidelines.Study Documentation and Record ManagementMaintain accurate study documentation including patient records, trial documentation, and regulatory files. Ensure proper filing and archiving of clinical trial documents.Participant and Data CoordinationAssist in collecting and managing study-related data and maintaining patient records according to research protocols. Ensure confidentiality and proper handling of patient information.Regulatory and Protocol ComplianceSupport compliance with clinical research regulations and institutional policies. Ensure study activities align with ethical guidelines and Good Clinical Practice standards.Collaboration with Research TeamsWork closely with investigators, clinical staff, and research coordinators to ensure efficient trial operations and timely completion of study tasks.Required QualificationsEducational RequirementsCandidates must have a Bachelor’s degree in Science such as B.Sc, B.Pharm, Biotechnology, Zoology, Botany, or other Life Sciences disciplines.A Postgraduate Diploma in Clinical Research is mandatory.Experience and SkillsBasic understanding of clinical research processes and clinical trial documentation. Strong organizational and communication skills are required for effective coordination of research activities. Candidates should demonstrate attention to detail, strong documentation skills, and the ability to collaborate with clinical and research teams.Age EligibilityMinimum Age Limit: 18 yearsMaximum Age Limit: 35 yearsSalary InsightsThe selected candidate will receive a consolidated salary of ₹33,600 per month as per institutional guidelines. This role provides valuable experience in clinical research and may open opportunities for career growth in clinical trials and research operations.Employment DetailsNumber of Posts: 01The position is contractual for six months from the date of joining and may be extended depending on project requirements and institutional needs. The number of available posts may increase or decrease based on the requirements of the centre.Interview DetailsWalk-in Interview Date: 18 March 2026Reporting Time: 09:30 AM – 10:30 AMInterview VenueHomi Bhabha Cancer Hospital & Research CentreAganampudi, Visakhapatnam – 530053Candidates should bring their updated resume, a recent passport-size photograph, a photocopy of PAN card, original educational certificates, and one set of self-attested copies of all certificates.Company OverviewTata Memorial Centre is one of India’s premier cancer treatment and research organizations dedicated to advanced oncology care, clinical research, and medical education.The institution operates specialized cancer hospitals and research centres across India, including Homi Bhabha Cancer Hospital & Research Centre, which focuses on cancer diagnosis, treatment, and clinical research. Through its clinical research programs, the centre contributes to the development of innovative cancer therapies and improves patient care through evidence-based medicine.FAQsWho can apply for this role?Candidates with a Bachelor’s degree in Life Sciences such as B.Sc or B.Pharm along with a Postgraduate Diploma in Clinical Research.Is experience required for this role?While prior clinical research experience is beneficial, candidates with relevant education and training can apply.What is the salary offered?The role offers a consolidated monthly salary of ₹33,600.Is this a permanent role?No, this is a contractual position for six months, which may be extended depending on project requirements.Application Tips• Prepare an updated resume highlighting your life sciences background and clinical research training• Clearly mention your Postgraduate Diploma in Clinical Research in the qualifications section• Bring original certificates and self-attested copies for verification• Highlight any internships or projects related to clinical trials or research coordination• Arrive early at the venue to complete registration before the interview beginsOfficial Notification Click Here
Why This Role MattersClinical Data Management is a critical component of modern clinical research, ensuring that data generated during clinical trials is accurate, reliable, and compliant with global regulatory standards. Proper management of clinical trial data helps researchers evaluate treatment safety and effectiveness while supporting regulatory approvals for new therapies. The Clinical Data Coordinator II role at ICON plc plays a vital part in supporting clinical trials by maintaining data quality, managing electronic case report forms, and coordinating data validation processes. Professionals in this role help ensure that clinical trial datasets are complete, accurate, and ready for statistical analysis.Working within a global clinical research environment, this position supports clinical data scientists and project teams in identifying and resolving data issues, reconciling study data, and maintaining compliance with international regulatory standards. For experienced professionals in clinical data management, this role offers an opportunity to contribute to the development of innovative therapies while working in a fast-paced and collaborative clinical research environment.Job DescriptionICON plc is seeking a Clinical Data Coordinator II to join its clinical data management team in Bangalore, India. The selected candidate will support clinical trial data operations by assisting with electronic case report form maintenance, managing clinical data reconciliation, and ensuring the accuracy and integrity of study datasets. The role involves collaborating with clinical data scientists, project teams, and functional management to track study progress and address data-related issues. The Clinical Data Coordinator II will also contribute to maintaining data validation specifications and study-specific procedures while ensuring that all clinical trial data complies with regulatory requirements and company standards.Key Features of the RoleOpportunity to work in global clinical trial data managementInvolvement in clinical trial data analysis and validation processesCollaboration with clinical data scientists and cross-functional research teamsExposure to electronic data capture systems used in clinical trialsParticipation in maintaining data integrity and regulatory complianceContribution to the development of innovative treatments and therapiesResponsibilitiesClinical Data Management SupportAssist the Data Management Study Lead in maintaining electronic case report forms and ensuring that study documentation remains updated throughout the clinical trial process. Support the development and maintenance of data validation specifications and study-specific procedures.Data Review and ReconciliationManage reconciliation of clinical and third-party data based on predefined edit specifications and data review plans. Ensure that discrepancies are identified and resolved to maintain high-quality clinical trial datasets.Study Metrics and ReportingTrack and communicate the status of study tasks and key metrics to clinical data scientists, project teams, and functional management. Provide updates on study progress and data-related activities.Data Issue ResolutionAddress data-related queries and recommend appropriate solutions to maintain data accuracy. Investigate root causes of data issues and implement corrective measures to prevent recurrence.Collaboration and CommunicationWork closely with cross-functional teams including clinical research professionals, data scientists, and project managers to ensure efficient data management processes across clinical studies.Required QualificationsEducational RequirementsBachelor’s degree in Life Sciences, Healthcare, or a related scientific discipline.Experience and SkillsMinimum of 5 years of relevant experience in clinical data management within the pharmaceutical, biotechnology, or clinical research industry. Strong understanding of clinical trial data processes and electronic data capture systems.Technical KnowledgeFamiliarity with clinical data management platforms such as Medidata Rave and Oracle Clinical Remote Data Capture or similar systems used in clinical research environments. Understanding of global regulatory standards including Good Clinical Practice is considered advantageous.Professional SkillsStrong attention to detail and the ability to manage complex clinical datasets. Excellent communication skills and the ability to collaborate effectively with cross-functional teams in a fast-paced clinical research environment. Ability to analyze clinical data issues and implement systematic solutions to maintain data quality.Salary InsightsAlthough the exact salary package has not been disclosed, Clinical Data Management roles in global clinical research organizations typically offer competitive compensation based on experience, expertise, and company policies. Additional benefits may include healthcare coverage, retirement planning programs, and employee wellness initiatives.Company OverviewICON plc is a global clinical research organization that provides healthcare intelligence and clinical development services to pharmaceutical, biotechnology, and medical device companies. The company specializes in clinical trial management, data analysis, and regulatory support to accelerate the development of new medicines and therapies. Through its global network of research professionals, ICON helps bring innovative treatments to patients while maintaining high standards of scientific excellence and regulatory compliance.ICON promotes an inclusive work culture that encourages innovation, collaboration, and professional development, enabling employees to contribute to meaningful advancements in healthcare and clinical research.FAQsWho can apply for this role?Candidates with a bachelor’s degree in Life Sciences or a related field and relevant experience in clinical data management.How much experience is required?Applicants should have approximately five years of experience in clinical data management within pharmaceutical or biotechnology industries.What tools are commonly used in this role?Clinical data management systems such as Medidata Rave, Oracle RDC, or other electronic data capture platforms are commonly used.Does the role involve working with clinical trials?Yes. The position supports data management activities for clinical trials and ensures data quality throughout the study lifecycle.Application TipsHighlight your experience in clinical data management and electronic data capture systems.Mention any experience working with Medidata Rave, Oracle RDC, or similar data management platforms.Demonstrate familiarity with clinical trial data review processes and reconciliation activities.Emphasize knowledge of regulatory standards such as ICH-GCP.Showcase your ability to collaborate with multidisciplinary clinical research teams.
ICSR Case Advisor - Pharmacovigilance
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 Doctors specializing in aesthetic and regenerative medicine play a key role in helping patients improve their appearance, restore tissue health, and enhance overall wellbeing. Through advanced non-surgical treatments and regenerative therapies, they support patients in achieving safe and effective aesthetic outcomes while promoting long-term skin and tissue regeneration.Job DescriptionSaheel Group is seeking a Medical Doctor Specialist in Aesthetic and Regenerative Medicine to join its team in Riyadh Region, Saudi Arabia. This role involves delivering advanced aesthetic treatments, regenerative therapies, and personalized patient care while working collaboratively with healthcare professionals to achieve optimal patient outcomes.Key Features of the Role• Position: Medical Doctor – Specialist in Aesthetic & Regenerative Medicine• Company: Saheel Group• Location: Riyadh Region, Saudi Arabia• Employment Type: Full-Time• Work Mode: On-siteResponsibilities• Provide consultations and assessments for aesthetic and regenerative treatments• Diagnose patient needs and develop personalized treatment plans• Perform aesthetic procedures including facial rejuvenation and cosmetic injectables• Deliver regenerative treatments such as PRP therapy and advanced skin rejuvenation procedures• Educate patients about treatment options, risks, and aftercare• Monitor treatment outcomes and ensure patient satisfaction• Stay updated with advancements in aesthetic and regenerative medicine• Collaborate with medical professionals to deliver integrated patient careRequired Qualification• Medical degree (MBBS or equivalent)• Specialization or certification in aesthetic medicine or regenerative medicine• Valid medical license to practice in Riyadh Region, Saudi ArabiaImportant Requirements• Expertise in aesthetic procedures such as facial rejuvenation and cosmetic injectables• Knowledge of regenerative medicine techniques including PRP therapy and stem cell treatments• Strong diagnostic and clinical assessment abilities• Excellent patient communication and consultation skills• Commitment to continuous learning and professional developmentWhat We Offer• Opportunity to work in a growing healthcare organization• Exposure to advanced aesthetic and regenerative treatments• Collaborative and professional clinical environment• Career growth and professional development opportunitiesExperience and Skills• Aesthetic medicine procedures and facial treatments• Regenerative therapies such as PRP and tissue regeneration techniques• Patient consultation and treatment planning• Clinical assessment and diagnosis• Strong interpersonal and patient communication skillsSalary Insights• Salary not specified in the job listing• Compensation typically depends on experience, specialization, and clinic performanceCompany OverviewSaheel Group is a dynamic organization based in Riyadh focused on empowering businesses and supporting innovation across multiple sectors. The company emphasizes excellence, sustainability, and high-quality services while fostering collaboration and professional growth.FAQsWhere is the job located?The position is based in the Riyadh Region of Saudi Arabia.What type of specialization is required?Candidates should have specialization or certifications in aesthetic or regenerative medicine.What treatments will the doctor perform?Procedures may include facial rejuvenation, cosmetic injectables, PRP therapy, and other regenerative treatments.Is prior experience required?Prior experience in aesthetic or regenerative medicine is highly desirable.Application Tips• Highlight certifications or training in aesthetic or regenerative medicine• Include experience with procedures such as PRP therapy or cosmetic injectables• Demonstrate strong patient consultation and communication skills• Mention clinical experience in dermatology, cosmetic medicine, or related specialties• Emphasize continuous learning and staying updated with new medical technologies
Clinical Data Management Executive
Why This Role MattersClinical Data Management (CDM) is a critical component of clinical research that ensures the accuracy, consistency, and integrity of clinical trial data. Proper data management enables pharmaceutical companies and research organizations to analyze clinical outcomes, evaluate drug safety and efficacy, and support regulatory submissions. The Clinical Data Management Executive role focuses on managing clinical trial data throughout the study lifecycle, including electronic case report form development, data validation, medical coding, and reconciliation activities. Professionals in this role ensure that clinical trial data is collected, reviewed, and maintained according to regulatory standards and Good Clinical Practice guidelines.By supporting data quality checks, query management, and clinical database activities, CDM professionals play an important role in maintaining reliable clinical data used in regulatory submissions and scientific research. For candidates with backgrounds in pharmacy, life sciences, or clinical research coordination, this role provides valuable exposure to global clinical trial data management processes.Job DescriptionLambda Therapeutic Research is seeking a Clinical Data Management Executive to support clinical trial data management activities at its Ahmedabad location. The selected candidate will be responsible for supporting electronic data capture processes, reviewing clinical data for accuracy, managing data queries, and assisting with clinical data management documentation. The role also involves medical coding activities, data reconciliation, and training related to clinical data management systems.The position requires collaboration with clinical research teams, data managers, and project stakeholders to ensure that clinical data is processed, validated, and maintained according to study protocols and regulatory requirements.Key Features of the Role• Opportunity to work in clinical data management within a global CRO• Exposure to electronic data capture systems and clinical trial databases• Involvement in eCRF development and clinical data validation processes• Participation in query management and data reconciliation activities• Collaboration with clinical research teams and data management professionals• Opportunity to contribute to clinical trial documentation and data quality initiativesResponsibilitieseCRF Development and Testing• Support development and configuration of electronic Case Report Forms for clinical trials• Participate in testing of eCRF functionality and ensure data capture aligns with study protocols• Assist in identifying and resolving system issues during testing phasesData Validation and Query Management• Perform data validation checks to ensure clinical trial data accuracy and completeness• Generate and manage data queries related to discrepancies or missing information• Work with site teams and clinical staff to resolve data queries within defined timelinesClinical Data Management Documentation• Support preparation and maintenance of clinical data management documents• Assist in developing documents such as Data Management Plans, Data Validation Plans, and electronic CRF completion guidelines• Ensure documentation is maintained according to regulatory and project requirementsData Reconciliation and Medical Coding• Support reconciliation of clinical trial data across different systems• Perform medical coding activities for clinical data using standardized terminology systems• Assist in reviewing coded data to ensure accuracy and consistencyTraining and System Support• Provide support and training to project teams regarding data management systems and processes• Assist in training related to electronic data capture tools and data entry procedures• Participate in process improvement initiatives within the data management functionRequired QualificationsEducational Requirements• M.Pharm (Pharmacology or Quality Assurance)• BDS, BAMS, or BHMS• M.Sc in Life Sciences or related healthcare fieldsExperience and Skills• Experience working as a Clinical Research Coordinator at the site level for late-phase clinical trials• Experience with clinical data management processes and data handling activities• Familiarity with electronic data capture systems and related clinical trial tools• Knowledge of clinical research guidelines and documentation practices• Strong attention to detail and analytical abilities• Ability to manage multiple tasks and maintain accurate documentationTechnical Skills• Experience with EDC systems used in clinical trials• Familiarity with systems such as IWRS, ePRO, or similar clinical research tools• Understanding of clinical database management and query resolution processes• Basic knowledge of medical coding and clinical data validation activitiesSalary InsightsThe compensation for this role ranges between ₹3,00,000 and ₹6,00,000 per year depending on experience, qualifications, and relevant technical expertise. Additional benefits may include exposure to global clinical research projects, training opportunities, and career growth within clinical data management and clinical research operations.Company OverviewLambda Therapeutic Research is a global full-service Clinical Research Organization headquartered in Ahmedabad, India. The organization provides comprehensive clinical research services to pharmaceutical, biotechnology, and generic drug companies worldwide. With research facilities and operational centers in multiple international locations including the United States, Canada, Spain, the United Kingdom, and Poland, Lambda Therapeutic Research supports global clinical trials and regulatory research initiatives. The organization focuses on delivering high-quality clinical research solutions while ensuring compliance with international regulatory standards and Good Clinical Practice guidelines.FAQsWho can apply for this role?Candidates with qualifications such as M.Pharm, BDS, BAMS, BHMS, or M.Sc in Life Sciences.What experience is required for this position?Applicants with site-level experience working as Clinical Research Coordinators in late-phase clinical trials are preferred.What type of work will the CDM Executive perform?The role involves clinical data management activities including eCRF development, data validation, query management, medical coding, and data reconciliation.Which tools are commonly used in this role?The role involves working with electronic data capture systems and tools such as IWRS, ePRO, and other clinical trial data platforms.What is the salary range for this position?The salary typically ranges between ₹3,00,000 and ₹6,00,000 per year depending on experience.Application Tips• Highlight experience working as a Clinical Research Coordinator or in clinical trials• Mention familiarity with EDC systems and clinical data management tools• Demonstrate knowledge of clinical trial documentation and data validation processes• Showcase experience in query management and data reconciliation activities• Emphasize attention to detail and ability to maintain high data quality standards
General Dentist
Why This Role MattersGeneral Dentists play a crucial role in improving oral health and preventing dental diseases within communities. By providing accessible dental care and education, they help improve the wellbeing of individuals, particularly in underserved populations such as school children and elderly patients.Job DescriptionAustralian Dental Foundation Inc is seeking a motivated General Dentist to join its Western Australian team in Perth, Western Australia, Australia. The role involves delivering dental care through mobile dental clinics across schools, aged care facilities, and community organizations, helping improve access to quality oral healthcare.Key Features of the Role• Position: General Dentist• Organization: Australian Dental Foundation Inc• Location: Perth, Western Australia, Australia• Employment Type: Full-Time or Part-Time• Workplace: Mobile dental clinics across the Perth metropolitan regionResponsibilities• Provide dental examinations, diagnosis, and treatment for patients• Deliver preventive, restorative, and general dental procedures• Provide oral health education to schools, aged care facilities, and communities• Support public health initiatives focused on improving oral health outcomes• Maintain accurate patient records and treatment documentation• Collaborate with Oral Health Therapists and Dental Assistants in mobile clinics• Follow infection control and safety standards during clinical proceduresRequired Qualification• Bachelor of Dental Surgery (BDS) or equivalent dental qualification• Registration with the Australian Health Practitioner Regulation Agency (AHPRA)Important Requirements• Passion for community health and public dental services• Interest in paediatric and aged care dentistry• Valid driver’s licence and reliable transportation for travel within metro Perth• Strong clinical, communication, and patient care skillsWhat We Offer• Competitive remuneration and supportive working conditions• Ongoing professional training and development programs• Graduate Development Program for newly qualified dentists• Monthly professional webinars and networking with a community of 50+ dentists• Friendly and collaborative team environment focused on community impactExperience and Skills• General dentistry and preventive dental care• Patient education and oral health promotion• Community healthcare delivery• Clinical diagnosis and treatment planning• Collaboration with dental healthcare teamsSalary Insights• Salary not specified in the listing• The organization offers competitive remuneration based on experience and role requirementsCompany OverviewAustralian Dental Foundation Inc is an Australian registered health promotion charity dedicated to improving oral health outcomes across the country and in selected developing nations. Through mobile dental clinics, the organization delivers dental treatment and oral health education to schools, aged care facilities, and community groups to reduce oral health inequalities and improve access to care.FAQsIs this role suitable for new graduates?Yes, both experienced and newly graduated dentists are encouraged to apply.What type of patients will the dentist treat?The role focuses on patients in schools, aged care facilities, and community organizations.Where will the services be delivered?Dental services are provided through mobile clinics across the Perth metropolitan area.Is travel required for the job?Yes, a valid driver’s licence and reliable transport are required to travel between service locations.Application Tips• Highlight your dental qualification and AHPRA registration• Mention interest or experience in paediatric or aged care dentistry• Emphasize community health experience or public health initiatives• Showcase strong patient care and communication skills• Include any volunteer or outreach dental work if applicable
Medical Data Abstractor
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
Associate Dentist
Why This Role MattersAssociate Dentists play a crucial role in delivering high-quality dental care, improving patient oral health, and contributing to the success of modern dental practices. Their expertise helps diagnose, treat, and prevent dental conditions while building long-term relationships with patients.Job DescriptionCasey Smiles is seeking a passionate Associate Dentist to join its thriving private dental practice in Cranbourne, Melbourne, Victoria, Australia. This role offers the opportunity to work in a high-end clinic with an established patient base, advanced dental technology, and mentorship from experienced clinicians including Dr Mo.Key Features of the Role• Position: Associate Dentist• Company: Casey Smiles• Location: Cranbourne, Melbourne, Victoria, Australia• Employment Type: Full-Time• Practice Type: Private Dental Practice• Facilities: Modern 6-chair clinic with advanced dental technologyResponsibilities• Perform general dental examinations and diagnoses• Provide treatments such as restorative, cosmetic, orthodontic, and implant dentistry• Develop personalized treatment plans for patients• Maintain accurate clinical records and treatment documentation• Educate patients on oral health and preventive care• Collaborate with dental assistants and hygienists for effective patient care• Follow infection control and dental safety protocolsRequired Qualification• Bachelor of Dental Surgery (BDS) or equivalent dental degree• Registration with Australian Health Practitioner Regulation Agency (AHPRA)Important Requirements• Strong commitment to clinical excellence and patient care• Excellent communication and patient relationship skills• Motivation to expand dental skills and clinical knowledge• Ability to work in a collaborative and high-performing dental teamWhat We Offer• Busy appointment schedule with an established patient base• Mentorship from internationally recognised clinician Dr Mo• Exposure to advanced procedures including General Anaesthetic (GA) cases• Modern purpose-built dental clinic with advanced equipment• Supportive and collaborative team culture• Opportunities to expand skills in general, cosmetic, orthodontic, and implant dentistryExperience and Skills• General and restorative dentistry• Cosmetic and aesthetic dental procedures• Patient consultation and treatment planning• Dental imaging and diagnostic tools• Team collaboration and patient communicationSalary Insights• Estimated annual salary: $600,000 – $800,000 per year• Income potential may vary depending on clinical workload and commission structureCompany OverviewCasey Smiles is a well-established private dental clinic located in Melbourne’s south-eastern suburbs. The practice is known for its high-end patient care, advanced dental technologies, and collaborative team environment that supports professional development and clinical excellence.FAQsWhat type of practice is this role in?It is a private dental practice with modern facilities and an established patient base.Is mentorship available?Yes, the role includes mentorship from internationally recognised clinician Dr Mo.What treatments are offered in the clinic?The practice provides general, cosmetic, orthodontic, and implant dentistry.Where is the job located?The role is based in Cranbourne, Melbourne, Victoria, Australia.Application Tips• Highlight your dental qualifications and AHPRA registration• Mention experience in general or cosmetic dentistry• Demonstrate strong communication and patient care skills• Emphasize willingness to learn advanced dental procedures• Showcase teamwork and clinical excellence in your application
Medical Coder Pharmacovigilance & Clinical Data Coding
Why This Role MattersMedical coding is a critical component of pharmacovigilance and clinical data management. Accurate coding of medical information ensures that adverse events, medical histories, and drug-related conditions are standardized using globally recognized medical dictionaries. This process enables reliable safety data analysis, signal detection, and regulatory reporting in clinical trials and post-marketing pharmacovigilance programs.The Medical Coder - Pharmacovigilance role focuses on coding clinical and safety data using standardized terminology systems such as MedDRA and ATC classifications. By ensuring consistency in medical coding across clinical databases, professionals in this role help maintain the integrity and reliability of clinical trial data.This position plays an important role in supporting pharmacovigilance operations, clinical data standardization, and safety monitoring activities. For professionals with experience in medical coding, clinical data management, or pharmacovigilance operations, the role offers an opportunity to work on global clinical research projects while contributing to drug safety and regulatory compliance.Job DescriptionVeeda Lifesciences is seeking a Medical Coder to support pharmacovigilance and clinical data management activities in a remote working environment.The selected candidate will be responsible for performing medical coding of adverse events, medical conditions, and drug-related information using standardized medical dictionaries. The role involves collaboration with clinical data managers, pharmacovigilance teams, and clinical scientists to ensure accurate and consistent coding across clinical study databases. The Medical Coder will also contribute to documentation, reporting, and training activities while ensuring that coding processes comply with internal procedures and industry standards.Key Features of the Role• Opportunity to work in pharmacovigilance and clinical data coding• Remote work environment with global project exposure• Involvement in adverse event and medical terminology coding• Collaboration with pharmacovigilance and clinical data management teams• Exposure to electronic data capture systems used in clinical trials• Opportunity to contribute to coding process improvements and training initiativesResponsibilitiesMedical Coding Activities• Perform medical coding for adverse events, medical history, and medical conditions using standardized terminology systems• Apply MedDRA coding for safety-related clinical data• Use ATC classification coding for drug-related information• Ensure coding activities follow approved medical dictionaries and sponsor guidelines• Maintain consistency and accuracy of coded terms across clinical study databasesClinical Data Management Support• Collaborate with clinical data managers, pharmacovigilance teams, and clinical scientists• Raise queries in electronic Case Report Forms or EDC systems for coding discrepancies• Review sponsor feedback and update coded medical terms accordingly• Ensure coding activities align with clinical data management standardsReporting and Documentation• Prepare medical coding reports and performance metrics• Monitor coding backlog and ensure timely completion of assigned tasks• Maintain documentation related to coding activities in accordance with SOPs and regulatory standardsTraining and Team Collaboration• Develop training materials related to medical coding activities• Provide on-the-job training and guidance for new team members• Participate in departmental meetings to improve coding workflows and best practicesRequired QualificationsEducational Requirements• Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or related healthcare fields• B.Pharm, M.Pharm, Pharm.D, or equivalent qualification preferredExperience and Skills• 2 to 4 years of experience in medical coding within pharmaceutical companies or CROs• Experience working with pharmacovigilance or clinical data management teams• Strong understanding of medical terminology and coding standards• Knowledge of clinical trial data management processes• Strong attention to detail and accuracy in coding activities• Excellent documentation and communication skillsTechnical Skills• MedDRA coding for adverse event classification• ATC coding for drug classification• Experience using electronic data capture systems such as Medidata Rave, Oracle Inform, or similar platforms• Familiarity with clinical database management and data review processesSalary InsightsAlthough the exact salary is not specified, Medical Coding roles in pharmacovigilance and clinical data management typically offer competitive compensation depending on experience, technical expertise, and project responsibilities. Additional benefits may include remote work flexibility, exposure to global clinical research projects, and professional growth opportunities in pharmacovigilance and data management.Company OverviewVeeda Lifesciences is a global clinical research organization providing services across clinical trials, bioequivalence studies, pharmacovigilance, and clinical data management. The organization supports pharmaceutical and biotechnology companies in developing safe and effective therapies through high-quality research and regulatory-compliant processes. With a strong focus on clinical research excellence and regulatory compliance, Veeda Lifesciences contributes to global drug development programs while ensuring patient safety and data integrity across clinical studies.FAQsWho can apply for this role?Candidates with Pharmacy or Life Sciences degrees such as B.Pharm, M.Pharm, Pharm.D, or related qualifications with experience in medical coding.What experience is required for this position?Applicants should have 2 to 4 years of experience in medical coding within pharmaceutical companies or CROs.Which coding systems are used in this role?The role primarily uses MedDRA coding for adverse events and ATC classification coding for drug-related data.Is experience with clinical data systems required?Yes. Experience with EDC systems such as Medidata Rave, Oracle Inform, or similar clinical trial platforms is preferred.Is this a remote position?Yes. The Medical Coder role is offered in a remote working mode.Application Tips• Highlight experience with MedDRA and ATC coding systems• Mention experience working in pharmacovigilance or clinical data management teams• Demonstrate familiarity with EDC platforms such as Medidata Rave or Oracle Inform• Showcase accuracy and attention to detail in medical coding tasks• Emphasize collaboration with clinical data managers and pharmacovigilance professionals
Dental Assistant
Why This Role MattersDental Assistants are essential to ensuring smooth clinical operations and high-quality patient care in dental practices. They support dentists during procedures, manage clinical instruments and patient records, and help create a comfortable environment for patients receiving treatment.Job DescriptionNational Dental Care is seeking Dental Assistants to join its modern dental practice in Maroochydore, Queensland, Australia on the Sunshine Coast. The role involves assisting clinicians with dental treatments, supporting administrative functions, and ensuring a positive patient experience in a technologically advanced dental clinic.Key Features of the Role• Position: Dental Assistant• Company: National Dental Care• Location: Maroochydore, Queensland, Australia• Employment Type: Full-Time, Part-Time, and Casual opportunities available• Work Mode: On-site dental clinicResponsibilities• Assist dentists during clinical procedures and patient treatments• Prepare and sterilize dental instruments and treatment rooms• Provide administrative and clinical support to dentists and hygienists• Maintain patient records and assist with appointment management• Ensure infection control and hygiene protocols are followed• Engage with patients professionally to ensure a positive experience• Support smooth day-to-day operations of the dental practiceRequired Qualification• Dental Assistant training or relevant healthcare experience (preferred but not mandatory)Important Requirements• Basic computer skills with proficiency in Microsoft Office• Experience using Dental 4 Windows (D4W) software is advantageous• Strong communication and organizational skills• Professional appearance and strong interpersonal skills• Ability to manage multiple tasks and work in a fast-paced clinic environmentWhat We Offer• Competitive remuneration packages and incentive programs• Ongoing training and professional development opportunities• Networking opportunities with dental professionals across Australia• Supportive and collaborative workplace culture• Opportunity to work with advanced dental technologies such as CBCT, scanners, and CEREC• Community engagement opportunities through volunteering and fundraisingExperience and Skills• Dental chairside assisting and patient care• Clinical sterilization and infection control procedures• Administrative support and patient record management• Communication and patient interaction skills• Time management and organizational skillsSalary Insights• Salary details were not specified in the job listing• Competitive remuneration and incentive schemes may be offeredCompany OverviewNational Dental Care is one of Australia’s largest dental service providers with a nationwide network of modern dental clinics. The organization employs nearly 1,000 dental professionals and focuses on advanced dental technologies, professional development, and delivering high-quality patient care across Australia.FAQsDo I need prior experience to apply?Previous dental assistant experience is preferred but not required.What types of employment are available?Full-time, part-time, and casual positions are available.What technologies are used in the clinic?The practice uses advanced technologies such as scanners, CBCT, and CEREC systems.Where is the job located?The position is based in Maroochydore on the Sunshine Coast, Queensland, Australia.Application Tips• Highlight any dental assisting or healthcare support experience• Mention familiarity with dental software such as Dental 4 Windows if applicable• Demonstrate strong organizational and communication skills• Include any certifications or training in dental assisting• Emphasize reliability, teamwork, and patient care experience