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 276–300 of 423 jobs
Brand Manager - Adult Vaccines
Gsk
Mumbai2-5 Years · Onsite25 SeptGSK’s Adult Vaccines Brand Manager role in Mumbai is a strategic commercial position responsible for shaping how adult immunization brands are positioned, promoted, and grown across India. As vaccines become a cornerstone of GSK’s infectious disease portfolio, this role directly influences market share, HCP engagement, and patient access. The Brand Manager partners with sales, medical, regulatory, market access, and creative agencies to translate insights into differentiated campaigns. It is a compelling opportunity for pharma marketing professionals who want to combine scientific literacy with omnichannel execution, competitive intelligence, and P&L ownership. The position offers high visibility within a global biopharma leader and a chance to build expertise in one of the fastest-evolving preventive healthcare categories.
Associate Director - Global Study Lead
Gsk
Bengaluru5+ Years · Hybrid25 SeptThis Associate Director–Global Study Lead role places you at the center of GSK’s clinical development engine in Bengaluru, leading the operational planning and delivery of a global clinical study. The position is pivotal to GSK’s mission of uniting science, technology, and talent to get ahead of disease, supporting therapeutic areas such as respiratory, immunology, oncology, HIV, and infectious diseases. You will work across clinical operations, data management, safety, regulatory, and external partners, translating asset strategy into flawless study execution. With visible impact on pipeline milestones and patient outcomes, this is a compelling opportunity for seasoned clinical operations professionals seeking global matrix leadership, process innovation, and a direct role in advancing GSK’s ambitious health impact goals.
Associate Manager, Externally Sponsored Research
Sanofi
Hyderabad5+ Years · Onsite25 SeptSanofi Business Operations (SBO) in Hyderabad seeks an Associate Manager, Externally Sponsored Research (ESR) to oversee investigator-sponsored studies and externally sponsored collaborations from concept submission through closeout. This role sits at the intersection of clinical research, medical governance, and operational excellence, ensuring that unsolicited research support requests are routed for scientific review and managed in compliance with Sanofi SOPs, ICH-GCP, and local regulations. It is critical to Sanofi's Specialty Care, Vaccines, General Medicines, and R&D pipelines because ESRs generate real-world evidence and expand research partnerships. The position offers deep exposure to global stakeholders, SRC coordination, study start-up, product supply, contracting, and audit readiness. For professionals with clinical trial project management experience, it is a compelling opportunity to build specialized expertise in externally sponsored research operations while contributing to compliant, timely delivery of studies that inform medical and commercial strategy.
R&D Global Regulatory Affairs CMC Lead
Sanofi
Hyderabad5+ Years · Onsite25 SeptSanofi’s Global Regulatory Affairs CMC & Device Organization seeks an R&D GRA CMC Lead in Hyderabad to shape regulatory strategies for pharmaceuticals, biologics, vaccines, and combination products. This senior role is central to Sanofi’s pipeline, bridging R&D, manufacturing, and health authorities such as the US FDA and EMA. The CMC Lead ensures dossiers meet global quality and compliance standards, accelerates approvals, and mitigates regulatory risks across the product lifecycle. As a strategic partner, the position influences cross-functional teams, regulatory policy, and digital innovation, including AI-enabled regulatory workflows. For experienced CMC professionals, this is a high-visibility opportunity to lead complex submissions, negotiate with regulators, and advance patient access to innovative therapies while growing within a world-class regulatory network.
Assistant Manager – Pharmacovigilance Local Case Intake (Japanese Language)
AstraZeneca
Bengaluru5+ Years · Onsite25 SeptAstraZeneca's Local Case Intake function is the front door of the company's patient-safety ecosystem, and this Assistant Manager role owns it for the Japanese market. Leading a team of Local Case Intake Advisors, you will make sure every adverse event report originating from Japanese Marketing Companies is captured, triaged, followed up and submitted within regulatory clocks. Because Japan is one of AstraZeneca's largest and most tightly regulated commercial markets, accuracy here directly protects licence continuity, Health Authority credibility and patient trust. This is a compelling next step for a pharmacovigilance professional with Japanese language capability who wants to move from individual case processing into people leadership, gaining structured exposure to PMDA interactions, Pharmacovigilance System Master File governance, inspection readiness and global safety transformation work inside a digitally enabled organisation.
Regulatory Affairs Manager
AstraZeneca
Mumbai5+ Years · Hybrid25 SeptAstraZeneca is seeking a Regulatory Affairs Manager in Mumbai to lead complex regulatory strategies for its innovative biopharmaceutical portfolio. This senior role sits at the intersection of science, compliance and commercial delivery, shaping submissions, lifecycle management and health-authority interactions across global and regional markets. The position is critical to accelerating patient access to medicines, ensuring filings are right first time and maintaining AstraZeneca’s reputation with regulators. You will advise cross-functional teams, mitigate regulatory risks and champion process improvements in a company known for scientific leadership. For an experienced regulatory professional, this is a high-visibility opportunity to influence pipeline decisions, mentor talent and work with global stakeholders. It offers a rare blend of strategic ownership, operational depth and career-defining exposure within one of the world’s leading patient-focused pharmaceutical companies.
Associate Manager - MSAT (Commissioning & Qualification)
Pfizer
Vizag5+ Years · Onsite25 SeptPfizer’s Manufacturing Science & Technology (MSAT) group at Vizag plays a critical role in commissioning, qualification and validation of sterile injectable manufacturing assets. The Associate Manager – MSAT (C&Q) ensures equipment, utilities, facilities and processes are qualified to cGMP, FDA and Pfizer Quality Standards, directly protecting product sterility, patient safety and regulatory compliance. This position matters because Vizag supports regulated-market injectables, where robust validation underpins every batch release. The role offers exposure to complex sterile processes, cleaning validation, computer system validation, audits and technology transfers. For pharma professionals with QA, validation or sterile manufacturing experience, it is a compelling opportunity to deepen technical expertise, work cross-functionally and influence compliance strategy at a global scale while building a pathway toward senior quality and MSAT leadership.
Market Access Specialist
Roche
Delhi NCR5+ Years · Hybrid25 SeptRoche is seeking a Market Access Specialist to join its Access & Policy team in New Delhi, with coverage across Delhi and Haryana. This senior role is central to Roche's mission of expanding equitable healthcare access in India across oncology, ophthalmology, rare diseases and neurology. The position shapes evidence-based, innovative programs that strengthen health systems, support state-level partnerships, and improve prevention, early detection, screening and quality of care for underserved populations. Working closely with State Access Partners, government bodies, public health organizations and internal cross-functional teams, the incumbent translates strategy into scalable, measurable impact. For professionals passionate about health policy, access and system transformation, this is a rare opportunity to influence public-private collaboration at scale while advancing a global leader's patient-access agenda in India.
Regulatory Affairs CMC Team Lead
Sanofi
Hyderabad5+ Years · Onsite25 SeptThis R&D GRA CMC Team Lead role at Sanofi in Hyderabad is a senior regulatory affairs leadership position within the Global Regulatory Affairs CMC & Device Organization. The incumbent will shape global Chemistry, Manufacturing, and Controls strategies for pharmaceuticals, biologics, vaccines, and combination products, directly influencing approval timelines and lifecycle management. As a critical bridge between technical development, manufacturing, and health authorities, this role ensures Sanofi's innovative therapies reach patients with speed and compliance. The position offers exceptional exposure to FDA, EMA, and other global regulators, matrixed project teams, and cutting-edge digital regulatory tools such as Veeva Vault. For regulatory professionals seeking to lead strategy, mentor specialists, and drive organizational change in a world-class biopharma environment, this is a compelling career step with significant influence on Sanofi's commercial and clinical pipeline.
Medical Science Liaison
Bayer
Delhi NCRFreshers · Onsite24 SeptServe as a scientific and medical liaison with healthcare professionals, thought leaders, medical societies, and other external stakeholders. The role focuses on scientific information exchange, medical education, advisory-board support, congress engagement, clinical-trial knowledge, and therapeutic-area insights.
Kit Production Assistant III
Labcorp
Bangalore2-5 Years · Onsite24 SeptSupport clinical research kit inventory operations by maintaining project and site-level Kit Material Supply systems, processing work orders, resolving kit-supply issues, supporting investigator sites, and ensuring accurate documentation and timely service delivery.
Clinical Study Manager II
ICON
Bangalore5+ Years · Hybrid24 SeptManage day-to-day clinical trial activities and lead planning, execution, monitoring, and issue resolution for complex clinical studies. The role supports sponsor-dedicated clinical development programmes while ensuring regulatory compliance, data integrity, quality, timelines, and efficient resource utilization.
Manager QA – EPD Quality Systems
Abbott
Mumbai5+ Years · Onsite24 SeptManage Quality Systems initiatives within Abbott's EPD Quality System organization, supporting Quality Management System processes with emphasis on Third-Party Manufacturer and Supplier Quality Management. The role drives continuous improvement, regulatory compliance, global initiatives, and quality-system governance.
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Scientific Writer II
Bristol Myers Squibb
Hyderabad2-5 Years · Onsite24 SeptAuthor and coordinate high-quality regulatory and clinical documents by integrating scientific, medical, and regulatory input across cross-functional development teams. The role combines scientific writing, document strategy, timeline management, quality review, and regulatory documentation expertise.
Senior Medical Advisor
Pfizer
Mumbai5+ Years · Onsite24 SeptProvide scientific and medical expertise to support medical strategy, launch readiness, evidence generation, and external engagement for Specialty Care and Internal Medicine pipeline products while ensuring scientific integrity and regulatory compliance.
Research Associate-R&D
Piramal Pharma Solutions
Ennore0-2 Years · Onsite24 SeptExecute analytical laboratory activities for R&D samples, supporting NMR, wet chemistry, spectroscopy, HPLC, and GC analysis while maintaining accurate laboratory records and complying with cGMP, GLP, SOP, and safety requirements.
Regulatory Publishing Specialist
Syneos Health
Delhi NCR2-5 Years · Remote24 SeptSupport the preparation, publishing, quality control, and submission of regulatory applications for global health authorities. The role requires hands-on electronic publishing expertise, strong attention to detail, and the ability to manage multiple regulatory projects concurrently.
Associate Clinical Data Coordinator
Iqvia
Thane0-2 Years · Onsite24 SeptSupport Clinical Data Management activities by coordinating study data operations, maintaining data quality, resolving data clarifications, and supporting database and testing activities. The role offers exposure to clinical data workflows, coding, audit activities, and cross-functional collaboration.
Key Account Manager - Aesthetics
AbbVie
India2-5 Years · Hybrid24 SeptDrive strategic account relationships, market access, and contracting for leading aesthetics brands at Allergan Aesthetics (AbbVie).
Associate - IC Plan Design
Amgen
Hyderabad2-5 Years · Onsite24 SeptDesign, model, and execute field incentive compensation plans and sales contests at Amgen Hyderabad.
Director, Process Development- Drug Product
Amgen
Hyderabad5+ Years · Onsite24 SeptLead and build the Drug Product Technologies organization at Amgen Hyderabad, driving process development, digital transformation, and global biotech deliverables.
Analyst - Dangerous Goods
Merck KGaA
Bangalore0-2 Years · Onsite24 SeptSupport the safe, compliant, and efficient movement of goods across global supply chains while applying scientific and regulatory expertise to Dangerous Goods activities. The role combines compliance, cross-functional collaboration, process improvement, and global project support.
Medical Governance Lead
Novartis
India5+ Years · Onsite24 SeptMedical Governance Lead accountable for strengthening governance, compliance, SOP adherence, MLR oversight, audit readiness and Managed Access Program governance across Medical Affairs activities in India.
Research Associate : Pharma Analytical
Lupin
Pune2-5 Years · Onsite24 SeptDrive analytical data management, software validation, and enterprise application implementation for R&D operations at Lupin Pune.
Head of Manufacturing and Supply Services Hyderabad Hub
Sanofi
Hyderabad5+ Years · Hybrid23 SeptLead and direct large-scale manufacturing and supply operations and teams (400+ personnel) at the Hyderabad Hub.