Clinical Research Jobs in Mumbai

Why This Role MattersClinical research plays a fundamental role in the development of new medicines, medical devices, and treatment strategies. Before a drug or therapy can be approved for patient use, it must undergo extensive clinical trials to evaluate its safety, efficacy, and overall therapeutic benefit. Clinical Research Associates (CRAs) are key professionals responsible for ensuring that these trials are conducted according to strict regulatory and ethical standards.The role of a Clinical Research Associate is critical in maintaining the quality and integrity of clinical trial data. CRAs act as the bridge between sponsors, research sites, investigators, and regulatory authorities. Their primary responsibility is to monitor clinical trial sites, verify data accuracy, and ensure compliance with international guidelines such as ICH-GCP.In modern clinical research, accurate documentation, proper site monitoring, and data verification are essential to ensure that clinical trial results are reliable and acceptable to regulatory authorities. CRAs ensure that study protocols are followed correctly, participant safety is maintained, and all clinical activities adhere to regulatory requirements.This role is especially valuable for professionals seeking a long-term career in clinical trials, contract research organizations (CROs), and pharmaceutical development. By gaining experience in monitoring, regulatory compliance, and clinical trial management, CRAs can build a strong career path in the global healthcare and pharmaceutical industry.Job DescriptionAnaZeal Analyticals and Research Pvt. Ltd. is hiring Clinical Research Associates to support clinical trial monitoring and site management activities. The role requires professionals who can ensure proper execution of clinical trials while maintaining compliance with regulatory standards and Good Clinical Practice guidelines.As a Clinical Research Associate, the selected candidate will be responsible for conducting site monitoring visits, reviewing clinical documentation, and verifying data accuracy through Source Data Verification processes. This includes ensuring that data recorded in electronic case report forms accurately reflects information recorded in source documents.The role also involves coordinating with investigators, sponsors, and clinical trial teams to ensure smooth study operations. CRAs are expected to monitor trial progress, identify potential issues, and provide solutions to maintain compliance and study timelines.Professionals in this role must maintain detailed monitoring reports, track regulatory documents, and support audit readiness. Ensuring that clinical trial documentation is complete and compliant is a key responsibility of the position.The job may require travel to clinical trial sites for monitoring visits, investigator meetings, and compliance assessments. Strong organizational skills, attention to detail, and effective communication abilities are essential to succeed in this position.Key Features of the Role:• Opportunity to work in a Clinical Research Organization (CRO) environment• Hands-on exposure to clinical trial monitoring and site management• Experience working with ICH-GCP regulatory guidelines• Direct interaction with investigators, sponsors, and clinical research teams• Field-based experience in real-world clinical trial environments• Career growth opportunities in clinical research and pharmaceutical developmentResponsibilities• Conduct site monitoring visits to ensure clinical trials are conducted according to protocol requirements.• Perform Source Data Verification (SDV) to confirm accuracy of clinical trial data.• Review study documentation including informed consent forms and regulatory files.• Ensure compliance with ICH-GCP guidelines and regulatory standards.• Coordinate with investigators, sponsors, and study teams to support clinical trial operations.• Submit monitoring visit reports within required timelines.• Identify site-related issues and work with the study team to resolve them.• Track study progress and ensure adherence to study protocols.• Review electronic Case Report Forms (eCRF) for completeness and accuracy.• Maintain proper documentation for clinical trial records.• Support site readiness for regulatory inspections and audits.• Assist in maintaining trial documentation in accordance with regulatory requirements.Required Qualifications• Strong understanding of clinical research processes and clinical trial monitoring• Knowledge of international regulatory guidelines including ICH-GCP• Excellent attention to detail and documentation accuracy• Strong communication and coordination abilities• Ability to manage multiple study sites and monitoring activitiesEducational Requirements:• Bachelor’s degree in Life Sciences• Bachelor’s degree in Pharmacy (B.Pharm)• Degree or certification in Clinical ResearchExperience and Skills:• 0.6 – 2 years of experience in clinical research or CRA roles• Hands-on experience in site monitoring and clinical trial coordination• Strong knowledge of Source Data Verification (SDV) processes• Familiarity with electronic Case Report Forms (eCRF) systems• Good understanding of regulatory documentation and compliance requirements• Ability to coordinate with investigators, sponsors, and clinical teams• Strong documentation review and reporting skills• Willingness to travel for clinical site visitsSalary InsightsFor Clinical Research Associate roles with 0–2 years of experience in India, the typical salary range is between ₹2.4 LPA and ₹4.2 LPA, depending on the candidate’s experience, monitoring exposure, and clinical research expertise.Additional benefits may include professional development programs, clinical research training, travel allowances for monitoring visits, and opportunities for career advancement in the CRO industry.Company OverviewAnaZeal Analyticals and Research Pvt. Ltd. operates in the Clinical Research Organization (CRO) sector, providing clinical trial support, research services, and regulatory compliance expertise. CROs play an essential role in assisting pharmaceutical companies and sponsors in conducting clinical trials efficiently and according to regulatory standards.By working with AnaZeal Analyticals and Research, professionals gain valuable exposure to clinical trial operations, regulatory compliance processes, and real-world monitoring activities. The organization focuses on maintaining high-quality research standards and ensuring that clinical studies are conducted ethically and accurately.FAQs1. What does a Clinical Research Associate do?A Clinical Research Associate monitors clinical trial sites, verifies data accuracy, ensures regulatory compliance, and supports the overall management of clinical trials.2. Is travel required for CRA jobs?Yes, many CRA roles require travel to clinical trial sites for monitoring visits and site management activities.3. What skills are important for a CRA role?Key skills include clinical trial monitoring, regulatory knowledge, documentation review, data verification, and communication with investigators and sponsors.4. What career growth opportunities exist after becoming a CRA?Professionals can advance to Senior CRA, Clinical Trial Manager, Clinical Project Manager, or Regulatory Affairs roles.Application Tips• Highlight your experience with site monitoring and Source Data Verification (SDV).• Mention your knowledge of ICH-GCP guidelines and regulatory compliance.• Include experience related to clinical trial documentation and eCRF systems.• Emphasize your communication skills and ability to coordinate with investigators.• Showcase any clinical research certifications or training programs.• Ensure your resume reflects your willingness to travel and manage site visits.

Why This Role MattersCroissance Clinical Research operates within the fast-growing Clinical Research Organization (CRO) sector, supporting pharmaceutical and healthcare companies in drug development and research services. Business Development plays a critical role in expanding partnerships, generating revenue, and strengthening long-term sponsor relationships.This position offers professionals with 1–2 years of experience an opportunity to transition into the strategic side of clinical research. If you are aiming to build a stable and growth-oriented career in the CRO industry, this role provides exposure to sponsor interactions, proposal strategy, and healthcare market expansion.Job DescriptionCroissance Clinical Research is inviting applications for the position of Business Development Executive in Mumbai. The selected candidate will be responsible for identifying business opportunities, developing client relationships, and supporting growth initiatives within the clinical research and pharmaceutical sectors.This role combines strategic communication, market research, and client engagement, making it ideal for candidates with a life sciences or pharmacy background who want to move beyond technical roles into business growth functions.Key Features of the Role• Opportunity to work in the Clinical Research Organization (CRO) sector• Exposure to pharma sponsors and healthcare clients• Direct involvement in proposal preparation and client presentations• Growth-oriented business development career path• Dynamic and collaborative work environment• Long-term career opportunities in clinical research servicesResponsibilities Required• Identifying new business opportunities in clinical research and pharma sectors• Developing and maintaining strong client relationships with sponsors and stakeholders• Supporting proposal preparation, costing discussions, and business presentations• Conducting market research to identify emerging opportunities in life sciences• Coordinating with internal operational teams to ensure seamless service delivery• Representing the organization at industry meetings and networking events• Tracking leads, follow-ups, and maintaining CRM data• Supporting revenue growth targets and business expansion strategiesQualificationsCandidates must possess one of the following qualifications:• Bachelor’s degree in Life Sciences• Bachelor’s degree in Pharmacy• Bachelor’s degree in Biotechnology• Degree in Healthcare or related discipline• Master’s degree in relevant field (preferred)• MBA (Marketing / Healthcare Management) preferred but not mandatoryEducational Requirements• Full-time degree from a recognized university• Strong academic background in healthcare or life sciences• Business or marketing specialization is an added advantageExperience and SkillsExperience• 1–2 years of experience in business development, pharma sales, or clinical research• Experience in CRO environment will be an added advantage• Fresh MBA graduates with internship exposure may also be consideredSkills Required• Strong communication and presentation skills• Client relationship management ability• Basic understanding of clinical trials and pharma industry structure• Market research and competitive analysis skills• Negotiation and persuasion capability• Professional networking skills• Self-motivated and target-driven attitudeSalary InsightsEstimated Salary Range• ₹3.0 LPA – ₹5.0 LPA (based on experience and performance)Additional Benefits:• Career growth opportunities in the clinical research industry• Exposure to pharma sponsors and CRO business models• Performance-based incentives (as per company policy)• Professional networking exposure• Skill development in strategic business functionsCompany OverviewCroissance Clinical Research is a Clinical Research Organization (CRO) providing research and development support services to pharmaceutical, biotechnology, and healthcare companies. CROs play a crucial role in clinical trials, regulatory submissions, and product development support.Working in a CRO environment offers structured exposure to global research standards, sponsor management, and regulatory compliance systems. The company focuses on delivering reliable clinical research services while building strong partnerships within the healthcare ecosystem.FAQsIs prior CRO experience mandatory?No, candidates with pharma sales or business development experience are also eligible.Is MBA compulsory?No, MBA is preferred but not mandatory.What type of career growth can be expected?Progression into Senior Business Development Executive, Business Development Manager, or Strategic Alliances roles.Is this a field-based or office-based role?The role may involve client meetings and networking events along with office coordination.Location of posting?Mumbai.Application Tips• Research basics of clinical research and CRO business models• Understand sponsor-CRO relationships• Prepare examples of client handling or sales achievements• Highlight communication and presentation skills in resume• Be ready to discuss revenue targets or business expansion ideas• Demonstrate knowledge of pharma industry trends

Why This Role MattersClinical trials are the foundation of medical innovation. In high-impact therapeutic areas such as Oncology and Immunology, precision, compliance, and patient safety are critical. Every monitoring visit, every data query resolved, and every protocol deviation addressed contributes to the development of potentially life-saving therapies.As a Clinical Research Associate (CRA) II at ICON plc, you play a direct role in ensuring that clinical trials are conducted ethically, safely, and in full compliance with regulatory standards. Your oversight ensures that complex oncology and immunology studies generate reliable data while protecting trial participants. This position is instrumental in advancing innovative treatments from development to regulatory approval.Job DescriptionThe Clinical Research Associate II is responsible for managing and monitoring assigned clinical trial sites in accordance with study protocols, sponsor expectations, ICH-GCP guidelines, and applicable regulatory requirements. This role requires strong on-site monitoring experience, therapeutic expertise in Oncology or Immunology, and the ability to independently manage site relationships.The CRA II acts as the primary liaison between the sponsor and investigational sites, ensuring that studies are conducted with integrity and operational efficiency. The role involves significant travel and requires strong organizational and communication skills to manage multiple responsibilities simultaneously.Key Features of the Role• Focus on Oncology and Immunology therapeutic areas• Independent on-site monitoring responsibilities• Exposure to complex, high-impact clinical trials• Significant travel opportunities (domestic and international)• Cross-functional collaboration with global teams• Career progression toward Senior CRA or Clinical Trial Manager roles• Compliance-driven and patient-focused environmentResponsibilities• Conduct site qualification, initiation, monitoring, and close-out visits in accordance with monitoring plans.• Ensure adherence to study protocols, ICH-GCP standards, and regulatory requirements.• Review source documents to verify data accuracy and completeness.• Ensure informed consent processes are conducted properly and documented accurately.• Monitor patient recruitment, enrollment progress, and retention metrics.• Identify protocol deviations, documentation gaps, and compliance risks.• Ensure timely and accurate reporting of adverse events and safety information.• Perform detailed data review and resolve queries in collaboration with site staff and data management teams.• Ensure case report forms (CRFs) are complete, accurate, and submitted within required timelines.• Collaborate with investigators and site personnel to facilitate smooth trial conduct.• Provide training and support to site staff regarding protocol requirements and study procedures.• Contribute to the preparation and review of essential study documentation, including protocols and clinical study reports.• Maintain accurate monitoring visit reports and follow-up documentation.• Manage multiple sites and ensure all milestones are met within study timelines.Required Qualifications• Strong understanding of clinical trial processes and lifecycle management.• In-depth knowledge of ICH-GCP guidelines and regulatory frameworks.• Proven experience in Oncology and/or Immunology therapeutic areas (mandatory).• Strong analytical skills for interpreting complex clinical data.• Excellent communication and stakeholder management abilities.• High attention to detail and documentation accuracy.• Ability to independently manage site activities and resolve issues proactively.Educational Requirements• Bachelor’s degree in Life Sciences, Pharmacy, Nursing, Medicine, Biotechnology, or related healthcare discipline.• Bachelor’s degree in Life Sciences, Pharmacy• Advanced clinical research certifications are an added advantage.Experience and Skills• Minimum 3 years of experience as a Clinical Research Associate.• Demonstrated on-site monitoring experience.• Experience handling Oncology or Immunology clinical trials (mandatory).• Strong administrative and documentation skills.• Proficiency in Clinical Trial Management Systems (CTMS) and Electronic Data Capture (EDC) platforms.• Experience managing safety reporting and regulatory documentation.• Ability to interpret clinical data and identify trends or discrepancies.• Strong problem-solving and risk mitigation skills.• Ability to work both independently and collaboratively within global teams.• Willingness and ability to travel at least 60% (domestic and international).• Valid driver’s license required.Salary InsightsCompensation for the Clinical Research Associate II role is competitive and aligned with industry benchmarks for Oncology-focused CRA positions. Salary may vary based on therapeutic expertise, travel flexibility, and geographic region.In addition to base salary, employees at ICON plc may receive:• Comprehensive health insurance coverage• Retirement savings programs• Performance-linked incentives• Annual leave entitlements• Life assurance benefits• Global Employee Assistance Programme (LifeWorks)• Flexible lifestyle and wellness benefitsICON’s total rewards framework supports career development, financial planning, and work-life balance.Company OverviewICON plc is a globally recognized leader in healthcare intelligence and clinical research services. The company partners with pharmaceutical, biotechnology, and medical device organizations to accelerate the development of innovative treatments across all phases of clinical development.With a strong presence worldwide, ICON supports complex clinical programs in therapeutic areas including Oncology and Immunology. The organization fosters an inclusive, performance-driven culture focused on scientific excellence and operational quality.Inclusion and belonging are core values at ICON. The company is committed to providing equal employment opportunities and maintaining a workplace free from discrimination and harassment.FAQs1. Is Oncology/Immunology experience mandatory?Yes, therapeutic area experience in Oncology or Immunology is mandatory for this role.2. Does this role require travel?Yes, the position requires approximately 60% travel, including domestic and international visits.3. Is on-site monitoring experience required?Yes, demonstrated on-site monitoring experience is essential.4. What growth opportunities are available?Career progression may include Senior CRA, Lead CRA, Clinical Trial Manager, or Project Management roles.5. Does this role involve data analysis?The role includes data review and query resolution but does not replace formal biostatistical analysis functions.Application Tips• Highlight Oncology/Immunology trial experience prominently in your resume.• Quantify monitoring experience (number of sites, visits conducted, countries supported).• Demonstrate strong knowledge of ICH-GCP and regulatory compliance.• Mention experience handling adverse event reporting and safety oversight.• Emphasize travel flexibility and independent site management capability.• Showcase examples of resolving complex site or data-related issues.

Roles & Responsibilities• Support clinical studies by coordinating study data and essential documents• Participate in the development and testing of case report forms (CRFs), databases, and study reports• Verify study data, resolve discrepancies, and ensure timely completion of study documentation• Process subject compensation and resolve related discrepancies• Create, organize, and maintain clinical study files and regulatory documentation• Assist during internal and external audits to ensure accuracy and completeness of study records• Communicate with internal teams and stakeholders for study updates and clarifications• Provide guidance and support to new or entry-level team members• Ensure compliance with established clinical research processes and regulatory requirementsQualification• Bachelor's degree in Pharmacy• Bachelor’s degree in Life Sciences or a related fieldExperience• Minimum 2 years of relevant experience in clinical research, data coordination, or document managementSkills• Strong organizational and time management skills• Good written and verbal communication abilities• Problem-solving and analytical skills• Ability to work under moderate supervision with structured processes• Familiarity with clinical data management systems and regulatory documentation preferredAbout the CompanyMedtronic is a global leader in healthcare technology, focused on developing innovative medical solutions that improve patient outcomes worldwide. The company operates across multiple therapeutic areas and is committed to advancing healthcare through research, collaboration, and technology-driven solutions.

Roles & Responsibilities• Support global study teams with Trial Master File (TMF) maintenance• Manage and update Veeva Vault, CTMS, and EDC systems• Assist in Ethics Committee (EC) and Health Authority (HA) submissions• Track essential documents and clinical trial milestones• Coordinate study meetings, training documentation, and trial communications• Support site start-up activities and regulatory document collection• Maintain inspection-ready documentation for audits and inspections• Liaise with vendors, internal teams, and site personnel• Ensure compliance with ICH-GCP and global regulatory standardsQualification• Bachelor of Pharmacy• Bachelor’s degree in Life Sciences / Pharmacy / Biotechnology or related fieldExperience• 1–2 years of experience as a Clinical Trial Assistant (CTA)• Hands-on experience in EC & HA submissions• Experience in site payments tracking and essential clinical documentationSkills• Strong understanding of ICH-GCP guidelines and global clinical operations• Proficiency in Veeva Vault, CTMS, and EDC platforms• Excellent documentation and organizational skills• Strong communication and coordination abilities• Ability to manage multiple tasks in a fast-paced global CRO environment• High attention to detail and compliance focusAbout the CompanyICON plc is a global Contract Research Organization (CRO) providing clinical development and commercialization services to pharmaceutical and biotechnology companies, supporting global clinical trials with regulatory excellence and operational expertise.

Roles & Responsibilities:• Track and identify clinical resource needs across projects• Manage staff assignments, availability, and project module updates• Maintain resourcing dashboards and forecasting tools• Forecast labor needs across different geographical regions• Identify and allocate staff based on therapeutic area expertise• Align resource assignments with client and project requirements• Update roll-off dates and staffing projections• Prepare utilization, forecasting, and projection reports using Excel and dashboards• Support RFP submissions and bid defense meetings with resourcing data• Track and distribute updated CVs for project allocation• Coordinate with internal departments for documentation and staffing updates• Support quality control of departmental reports and resource documentationQualification:• Bachelor of Pharmacy• Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related field preferred• Equivalent education and training combinations consideredExperience:• 0–2 years of relevant experience in clinical operations, resourcing, or data analysisSkills:• Proficiency in MS Office (Advanced Excel & Outlook preferred)• Strong quantitative and analytical abilities• Excellent attention to detail and accuracy• Ability to manage multiple projects simultaneously• Strong written and verbal communication skills• Basic understanding of clinical trial operations (preferred)About the Organization:Thermo Fisher Scientific, through its PPD clinical research services, is a global leader in life sciences and clinical research solutions, supporting pharmaceutical and biotech companies across the drug development lifecycle.

Roles & Responsibilities• Perform site monitoring visits (selection, initiation, monitoring, and close-out visits) in accordance with GCP and ICH guidelines.• Work with sites to drive and track subject recruitment plans to meet project needs and enhance predictability.• Administer protocol and related study training to assigned sites and establish regular communication to manage project expectations and issues.• Evaluate the quality and integrity of study site practices and adherence to regulations, escalating quality issues as necessary.• Track the progress of assigned studies, including regulatory submissions, recruitment, CRF completion, and data query resolution.• Ensure site documents are available for filing in the Trial Master File (TMF) and ensure Investigator's Site File (ISF) is maintained according to GCP/ICH and local requirements.• Create and maintain documentation regarding site management and monitoring visit findings, submitting regular reports and follow-up letters.• Collaborate with study team members for project execution support as needed.• If applicable, support development of site-specific subject recruitment plans and manage site financials per clinical trial agreements.Qualification• Relevant qualification in life sciences, clinical research, or related fields.Experience• 3+ years of relevant experience in Clinical Research.Vacancies• Multiple positions available in Bangalore, Mumbai, Ahmedabad, and Delhi.Skills• Strong knowledge of GCP, ICH, and regulatory guidelines.• Excellent communication and interpersonal skills.• Ability to manage site monitoring, recruitment, and data queries effectively.• Experience with Trial Master File (TMF) and Investigator's Site File (ISF).• Strong organizational skills and ability to track study progress.About the CompanyIQVIA India is a global leader in healthcare data and analytics, providing solutions to help clients in the pharmaceutical, biotechnology, and healthcare industries. IQVIA’s mission is to enable healthcare organizations to navigate complex data, deliver insights, and improve patient outcomes through advanced technology and clinical expertise.

Roles & Responsibilities• Coordinate day-to-day activities of Phase II oncology clinical trials• Assist investigators in protocol implementation and study documentation• Maintain Clinical Trial Files (CTF), CRFs, and essential regulatory documents• Ensure compliance with ICH-GCP, ethics committee, and sponsor requirements• Support patient recruitment, informed consent process, and follow-up visits• Manage data collection, query resolution, and study tracking activities• Liaise with clinical teams, study monitors, and regulatory authorities• Support multicentric and investigator-initiated oncology trialsQualification• B.Sc / B.Pharm / Graduate in Life Sciences• PG Diploma in Clinical Research – MandatoryExperience• Minimum 1 year of clinical research experience• Oncology trial exposure preferredAge Limit• Up to 35 yearsNo. of Post: 02Skills• Knowledge of ICH-GCP and clinical trial regulations• Strong documentation and regulatory file management skills• Good coordination and communication abilities• Attention to detail and compliance orientation• Ability to manage patient scheduling and trial timelinesWalk-In Interview Details(As per official notification by Tata Memorial Hospital – candidates are advised to refer to the official advertisement for date, time, and venue details.)About the OrganizationTata Memorial Hospital (TMC) is a premier cancer treatment and research institute under the Department of Atomic Energy, Government of India, known for its leadership in oncology care, clinical research, and advanced cancer therapies across India.OFFICIAL NOTICE CLICK HERE

Roles & Responsibilities• Develop detailed validation test plans for IRT (Interactive Response Technology) systems• Execute validation test plans and prepare validation documentation packages• Review requirement specification documents from internal stakeholders• Review and verify validation documents prepared by team members• Validate new IRT projects and updates to existing randomization and drug supply systems• Ensure validation activities are completed within defined timelines and quality standards• Support clinical trial randomization, investigational product management, and regulatory complianceQualification• Bachelor’s degree in Mathematics, Computer Science, or related fieldExperience• Experience in clinical trial data management, system validation, or software testing preferred• Exposure to IRT / IVRS / IWRS systems is an added advantageSkills• Strong analytical and problem-solving abilities• Knowledge of system validation and documentation standards• High attention to detail and quality compliance• Ability to manage tasks within strict timelines• Good written and spoken English communication• Team collaboration and cross-functional coordination skillsAbout the OrganizationMedpace is a global Clinical Research Organization (CRO) headquartered in Cincinnati, Ohio, operating in over 40 countries with 5,000+ employees. The company provides comprehensive clinical development services across multiple therapeutic areas and is recognized by Forbes and CRO Leadership Awards for its excellence in clinical research.

Roles & Responsibilities• Provide end-to-end oversight of animal health clinical trials from study set-up to completion• Obtain comprehensive understanding of study protocols, objectives, timelines, and deliverables• Define roles and responsibilities of study personnel and ensure alignment across teams• Collaborate with sponsors to establish and manage projected study timelines• Oversee execution of study activities to ensure tasks are completed accurately and on time• Manage GCP-compliant late-phase clinical trials in animal health• Review and contribute to study protocols, amendments, and final study reports• Monitor study progress, risks, and issues, ensuring timely escalation and resolution• Work cross-functionally with internal teams and external stakeholders to support study delivery• Ensure high standards of data quality, compliance, and documentation throughout the trial lifecycleQualification• Degree in Life Sciences, Veterinary Sciences, Pharmacy, or related disciplineExperience• Minimum 8+ years of clinical trial management experience within a CRO or animal health pharmaceutical organization• Proven experience managing GCP-compliant late-phase animal health clinical trials• Hands-on experience in protocol development and final study report writingSkills• Strong clinical trial management and leadership skills• High attention to detail with strong analytical mindset• Excellent time management and multitasking ability• Strong communication and stakeholder management skills• Dependability, flexibility, and ability to work effectively in team environments• Customer-centric and solution-oriented approachAbout the CompanyArgenta is a global animal health contract research and contract development and manufacturing organization (CRO/CDMO) dedicated exclusively to improving the lives of animals. Founded in 2006, Argenta partners with animal health companies worldwide, providing end-to-end solutions from molecule to market, supported by a strong culture of teamwork, innovation, customer focus, and global collaboration.

Roles & Responsibilities• Lead and line-manage a team of Clinical Research Associates (CRAs) based in Navi Mumbai• Recruit, onboard, train, and continuously develop CRAs to meet organizational standards• Oversee and guide CRAs to ensure high-quality delivery of core clinical monitoring responsibilities• Conduct regular one-to-one coaching sessions and provide constructive performance feedback• Track and manage CRA resourcing, workload allocation, and assignment planning• Support CRA engagement, retention, and career development aligned with company objectives• Collaborate with regional and local operations and cross-functional teams• Work closely with senior leadership to build and scale the clinical monitoring team in India• Travel for on-site evaluation and support of CRAs as required (approximately 10%)Qualification• Bachelor’s degree or higher in Life Sciences or a related disciplineExperience• 1–2 years of experience as a line manager or• Minimum 4 years of clinical monitoring experience as a CRA with readiness to move into line management• Prior experience in a global CRO preferredSkills• Strong leadership, mentoring, and people management skills• Advanced knowledge of Good Clinical Practice (GCP)• Excellent written and verbal communication skills• Ability to motivate, engage, and develop clinical research professionals• Strong organizational and resource management skills• Willingness to travel for CRA evaluationsAbout the CompanyMedpace is a full-service global clinical contract research organization providing Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device companies.

Roles & Responsibilities:• Prepare and review aggregate safety reports for global regulatory submissions including DSURs, PSURs, PADERs, Annual Reports, and RMPs• Lead report planning activities including data collection, kick-off meetings, and comment resolution discussions• Perform quality review of reports prepared by junior writers and provide feedback• Prepare benefit-risk evaluation documents, ad-hoc safety reports, and label update justifications• Write CTD summaries, clinical summaries, and regulatory submission documents• Draft adverse event narratives and medical information responses for healthcare professionals• Support signal detection activities and safety issue analysis• Conduct literature searches and summarize scientific findings• Collaborate with cross-functional teams and clients to ensure timely and high-quality deliverables• Ensure compliance with ICH-GCP guidelines, pharmacovigilance standards, and regulatory requirementsQualification:• Bachelor’s degree in Life Sciences or related field• Advanced degree (M.Sc., M.Pharm, PhD) preferredExperience:• Minimum 3 years of pharmaceutical industry experience• At least 2 years of experience in medical or safety writing preferred• Experience in regulatory submissions and pharmacovigilance documentation preferredSkills:• Strong knowledge of aggregate safety reporting and regulatory documentation• Understanding of pharmacovigilance practices, ICH-GCP guidelines, and global regulatory requirements• Excellent scientific writing, editing, and literature review skills• Proficiency in MS Office and document management systems• Strong organizational, communication, and time management skills• Ability to work collaboratively in global cross-functional teamsAbout the Organization:Fortrea is a global contract research organization providing clinical development, patient access, and pharmacovigilance solutions to pharmaceutical, biotechnology, and medical device companies. The organization focuses on delivering high-quality clinical and regulatory support to accelerate the development of life-saving therapies worldwide.

Roles & Responsibilities• Design, execute, and optimize integrated marketing campaigns across the provider journey to meet business objectives• Orchestrate delivery of campaign plans aligned with overall marketing strategy• Manage campaign calendars, timelines, and annual marketing plans• Lead tactic sequencing, prioritization, and end-to-end project management• Guide content strategy and messaging across media, web, email, sales tools, events, and other channels• Manage audience marketing budgets including media, agencies, and creative partners• Analyze campaign performance data and report KPIs and insights to drive optimization• Manage third-party vendors and internal channel partners for campaign execution• Collaborate with Product Management and Product Marketing teams on goals, market sizing, and positioning• Lead recurring stakeholder meetings to ensure timely and accurate campaign execution• Partner cross-functionally with Sales, Medical Affairs, Science, and Operations teams• Apply journey-based marketing strategies to deliver the right message at the right time• Ensure consistent brand experience, voice, and visuals across all marketing channelsQualification• Bachelor’s degree in Science or related disciplineExperience• 10+ years of marketing experience within healthcare or pharmaceutical industry• Experience in biopharmaceutical or oncology segment preferredSkills• Strong expertise in multi-channel and omni-channel marketing strategies• Deep understanding of customer journey and audience targeting• Knowledge of account-based marketing (ABM)• Strong experience with marketing automation tools, especially Eloqua• Working knowledge of CRM databases• Understanding of digital marketing technologies and AI platforms• Strong communication, copywriting, and editing skills• Excellent project management, organization, and data analysis skills• Ability to work effectively in a highly matrixed, global environment• Open to working across time zonesAbout the OrganizationLabcorp is a global leader in life sciences and diagnostics, supporting healthcare decisions through advanced laboratory services and integrated clinical solutions. The organization is committed to innovation, inclusion, and delivering high-quality outcomes for patients, providers, and partners worldwide.

Roles & Responsibilities• Perform independent EDC programming activities using Medidata RAVE across multiple studies with minimal supervision• Develop and implement solutions for global technical issues related to EDC tools such as Medidata RAVE and Veeva• Review and understand protocol, requirement documents, specifications, database and report designs• Create CRF annotations and programming specifications for dataset generation as per CDISC, transfer guidelines, and client standards• Produce Define XML/PDFs, annotated eCRFs, and Reviewer’s Guides for regulatory submissions• Develop visual analytics dashboards using tools such as Spotfire or Tableau• Implement post-production changes including edit checks, listings, protocol deviations, safety gateway, and RTSM (Balance) mappings• Program and validate datasets, edit checks, and quality checks; communicate data issues to Data Management• Perform database build reconciliation, project file review, listings, and documentation checks for accuracy and completeness• Ensure compliance with GCP and regulations related to computerized systems• Plan and oversee study-level programming activities including timelines, quality, resource estimation, and stakeholder coordination• Train and mentor team members on EDC tools to enable independent day-to-day operations• Interact with cross-functional teams and clients to resolve operational and technical issues• Work independently across multiple sponsors and proactively take on new challenges• Deliver work within agreed timelines and study budgets as per Fortrea SOPs and work instructionsQualification• University or college degree in Life Sciences, Health Sciences, Information Technology, or related field• Equivalent education and relevant work experience may be considered in lieu of a formal degreeExperience• 4–7 years of relevant clinical programming experience• Minimum 2 years of experience in protocol interpretation and EDC study buildSkills• Strong expertise in Medidata RAVE and EDC programming• Good understanding of clinical trial processes, data management, biometrics, and clinical systems• Experience with CDISC standards and submission deliverables• Strong analytical, problem-solving, and troubleshooting skills• Ability to work independently with minimal supervision• Strong communication, time management, and prioritization skills• Team-oriented mindset with the ability to handle multiple projects and tight deadlinesAbout the CompanyFortrea is a leading global clinical research organization specializing in clinical development, data management, and pharmacovigilance services. With a strong focus on innovation, regulatory compliance, and advanced clinical technologies, Fortrea partners with biopharmaceutical companies worldwide to deliver high-quality clinical trials and data-driven solutions across the drug development lifecycle.