Pharma, Clinical Research & Healthcare Jobs in India
511 open roles from pharma companies, CROs and hospitals, with new openings added most days. Apply directly through each employer's own page or contact.
Showing 301–325 of 423 jobs
Medical Data Reviewer
ICON
Bangalore2-5 Years · Remote23 SeptProvide expert medical oversight of clinical trial data, ensuring accuracy, consistency, and patient safety in a sponsor-dedicated model.
Clinical Data Coordinator II (CDC II)
ICON
Bangalore2-5 Years · Hybrid23 SeptDeliver high-quality clinical data management tasks, maintaining eCRFs, data validation specifications, and supporting study metrics.
Safety & PV Coordinator
Syneos Health
Hyderabad0-2 Years · Onsite23 SeptProcess ICSRs, perform safety tracking, and manage pharmacovigilance operations in an office-based role in Hyderabad.
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Speciality Care Advisor - Cardiology (field based in Mumbai)
Bristol Myers Squibb
Mumbai5+ Years · Onsite23 SeptDrive territory performance for Cardiology by identifying and mapping healthcare accounts, engaging healthcare professionals, supporting scientific activities and executing commercial strategies in line with BMS objectives and values.
Clinical Document Agent (2nd Shift - 2 PM to 11 PM IST)
Syneos Health
Remote2-5 Years · Remote23 SeptCreate and manage clinical project documentation, subject files and electronic documentation while converting raw study data into electronic formats and ensuring compliance with established clinical procedures and quality requirements.
Director, Process Development - Drug Product
Amgen
Hyderabad5+ Years · Onsite23 SeptLead the establishment and growth of Amgen's Drug Product Technologies organization in Hyderabad, building a high-performing team and operating model while expanding global drug product process-development capabilities through technical, digital and cross-functional innovation.
Associate- Quality Complaints
Amgen
Hyderabad2-5 Years · Onsite23 SeptManage assigned product complaint records and investigation activities within Amgen's global quality complaint process, ensuring procedural compliance, record quality, timely closure and continuous improvement.
Sr Professional Quality Management
Syneos Health
Hyderabad2-5 Years · Hybrid22 SeptSr Professional Quality Management Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. Job Responsibilities Job Summary Performs various activities (analysis, investigation, reporting, administration) related to ‘GXP’ (e.g. Good Clinical Practice or Good Pharmacovigilance Practice) and related topics for Clinical departments (therapeutic areas and functions).
Associate Manager SRC Governance
Sanofi
Hyderabad5+ Years · Hybrid22 SeptOur Team: Sanofi Business Operations (SBO) is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. Main responsibilities: Committee review Governance team support to set up governance to review meetings for all 4 committee reviews for ESRs, Phase 1 studies, Global Health Studies and MRPTC as per the established operating model. Study Review Committee (SRC) Primary responsibility is to Set up governance to review approval meetings for all 4 committee reviews - Company Sponsored Studies & Externally Sponsored Collaborations (CSS & ESC), ISS, Global Health Studies as per the established operating model. Identify stakeholders, organize pre-SRC meetings, maintain Action Registers, and manage audit readiness. Medico-Regulatory Pharmacovigilance Transversal Committee (MRPTC) Lead the conduct of the MRPTC including preparatory meetings, minutes, follow-up, and stakeholder coordination. Phase I SRC Set up governance for Phase 1 study review approval meetings, ensure cross-functional alignment, and manage risks and timelines.
Medical Affairs Manager
Johnson & Johnson
Mumbai5+ Years · Hybrid22 SeptMedical Affairs leadership role supporting DePuy Synthes country strategy, evidence generation, stakeholder engagement, innovation and medical/scientific activities.
Executive - Regulatory Affairs
Sun Pharmaceutical Industries Ltd
Panoli2-5 Years · Onsite22 SeptSupport plant and corporate Regulatory Affairs activities for global pharmaceutical submissions, GMP documentation and QMS coordination, with a focus on accurate compilation, review and timely execution of regulatory deliverables.
Regional Manager - Coronary & Renal Denervation
Medtronic
Hyderabad5+ Years · Remote22 SeptLead and coach a regional sales team to drive commercial growth and market adoption of advanced coronary and cardiovascular medical technologies at Medtronic.
Manager Regulatory Affairs
Abbott
Mumbai5+ Years · Onsite22 SeptExperienced Regulatory Affairs professional responsible for product registration submissions, regulatory strategy, agency interactions, lifecycle management, and regulatory support for established pharmaceutical products.
Clinical Trial Manager
Astellas
Bangalore2-5 Years · Hybrid22 SeptClinical Trial Manager responsible for planning, setting up, and executing assigned clinical trials while coordinating cross-functional teams, vendors, investigators, sites, budgets, timelines, and trial deliverables in compliance with GCP, ICH, SOPs, and regulatory requirements.
Senior Healthcare Executive
Pfizer
Chennai2-5 Years · Onsite22 SeptField-based healthcare sales role responsible for achieving territory sales targets, customer engagement, product promotion, market intelligence, and compliant execution of Pfizer commercial activities.
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Medical Science Liaison – Haematology & Oncology (field based in Kolkata)
Bristol Myers Squibb
Kolkata0-2 Years · Onsite22 SeptField-based Medical Science Liaison role supporting Haematology and Oncology through scientific engagement with Thought Leaders and Healthcare Providers. The role focuses on medical insights, evidence-based scientific dialogue, clinical trial support, pharmacovigilance, and execution of the country medical strategy.
Director, Global Clinical Trial Services, India
Regeneron
Hyderabad5+ Years · Onsite22 SeptDirector-level clinical operations leadership role responsible for clinical trial delivery across India, from feasibility through site close. The position leads India-based teams and FSP partners while coordinating with global functional leaders, sites, investigators, vendors, and regulatory authorities.
Regulatory Labeling Mgr
Amgen
Hyderabad5+ Years · Onsite21 SeptSupport the planning, coordination, and execution of EU and global labelling compliance activities within the Regulatory Affairs organisation.
Senior Clinical Trial Manager (Sr. CTM) - Internal Medicine
Thermo Fisher Scientific
Mumbai5+ Years · Remote21 SeptSenior Clinical Trial Manager responsible for end-to-end clinical trial start-up and clinical deliverables for moderate-to-high complexity studies across Internal Medicine and related therapeutic areas.
Study Grant Analyst II
Parexel
Hyderabad2-5 Years · Remote21 SeptStudy Grant Analyst II responsible for developing and analyzing clinical study grants for Phase I-IV trials, supporting pre-sales proposals and awarded projects, and ensuring compliance with fair market value and healthcare regulations.
Global Executive Assistant Capability Support Specialist
Sanofi
Hyderabad2-5 Years · Onsite21 SeptProvides high-level administrative, coordination, and talent acquisition support to Sanofi's Global Executive Development and Global Capability teams. The role focuses on executive calendar management, travel, meetings, purchasing, vendor coordination, communications, and confidential information handling.
MSL Oncology West
Bayer
Thane0-2 Years · Onsite21 SeptThe Medical Science Liaison will serve as a scientific and medical resource for oncology thought leaders across the West region. The role focuses on scientific exchange, clinical-trial support, medical education, advisory boards, congress engagement, and strategic thought-leader engagement.
Associate, Associate Database Analyst, Clinical Database Management
Pfizer
ChennaiFreshers · Hybrid21 SeptAssociate-level Clinical Database Management role supporting data monitoring, query management, database design, clinical data systems, documentation quality, and process improvement.
Clinical Trial Vendor Manager
Lupin
Pune5+ Years · Onsite21 SeptSenior clinical research role responsible for selecting, contracting, overseeing, and governing external vendors supporting clinical trials. The position focuses on quality, timelines, budgets, regulatory compliance, GCP standards, and vendor performance.
Specialist Quality Assurance Auditor – Innovative Medicine
Johnson & Johnson
Mumbai2-5 Years · Onsite21 SeptQuality Assurance specialist focused on R&D and Pharmacovigilance auditing, regulatory inspection support, GxP compliance, and quality systems. The role requires hands-on PV experience and supports audits across global healthcare operations.