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 151–175 of 249 jobs
Senior Statistical Programmer
Sanofi
Hyderabad5+ Years · Onsite25 SeptSanofi's Business Operations hub in Hyderabad anchors a global network of centralized statistical, medical and commercial capabilities serving Specialty Care, Vaccines, General Medicines, Consumer Healthcare and R&D. Within that structure, the Senior Statistical Programmer is a linchpin of Medical Affairs biostatistics — converting raw clinical trial and registry data into rigorous, QC'd tables, figures and listings that underpin abstracts, posters, manuscripts and regulatory-grade evidence. The position sits at the intersection of statistical science and programming craft, giving the holder direct exposure to Sanofi's global portfolio and to senior biostatisticians across geographies. For experienced SAS programmers who want their code to shape how medicines are described to physicians, regulators and payers worldwide, this is a rare chance to combine deep technical work with visible scientific impact.
Principal Statistical Programmer
Sanofi
Hyderabad5+ Years · Hybrid25 SeptSanofi Business Operations in Hyderabad is an internal global capability hub that centralises biostatistics, medical affairs and HEVA support for Sanofi's Specialty Care, Vaccines, General Medicines and R&D franchises. As a Principal Statistical Programmer, you become the technical anchor for statistical outputs that reach regulators, payers and physicians — transforming raw clinical trial and registry data into QC'd tables, figures and listings that underpin abstracts, posters, manuscripts and ad-hoc analyses. This is a genuinely strategic role: the quality of your SDTM and ADaM datasets directly influences how convincingly Sanofi communicates evidence for its pipeline. It is a compelling opportunity for an experienced programmer who wants global stakeholder exposure, formal mentorship responsibilities and the autonomy to design non-routine macros and advanced analytical techniques inside a world-class life-sciences environment.
Senior Biostatistician II
AstraZeneca
Bengaluru5+ Years · Hybrid25 SeptAt AstraZeneca, the Senior Statistician II role sits within the Biometrics and Statistical Innovation function, supporting late-phase oncology trials and regulatory submissions. This position is central to translating complex clinical questions into rigorous statistical designs, ensuring every protocol, analysis and dataset can withstand health authority scrutiny. The statistician partners with clinicians, translational scientists and data experts to generate reliable evidence across a rich pipeline of high-quality molecules and multiple indications. Because oncology trials often rely on time-to-event endpoints, this role directly influences how survival benefits are measured and communicated. It is a compelling opportunity for an experienced biostatistician to work at the intersection of modern science and advanced analytics, with strong investment in methods innovation, global academic collaborations and a culture that values curiosity, collaboration and smart risk-taking. Hybrid working in Bangalore adds flexibility.
Regional Medical Advisor – Oncology (Breast Cancer)
AstraZeneca
Bengaluru5+ Years · Hybrid25 SeptAstraZeneca's Regional Medical Advisor – Oncology (Breast Cancer) is a field-based scientific leadership position anchoring the company's medical strategy across Karnataka. As the recognised scientific expert for the breast cancer portfolio in the region, the advisor translates complex clinical and health-economic evidence into credible peer-to-peer dialogue with oncologists, pathologists, government bodies, patient advocacy groups and payer stakeholders. The role matters clinically and commercially: breast cancer remains one of AstraZeneca's flagship franchises, and scientifically informed engagement directly shapes guideline adoption, investigator-sponsored research and equitable patient access. For candidates, this is a rare platform combining deep therapeutic-area ownership, evidence-generation exposure and cross-functional visibility with global medical, clinical development and market access teams — a strong springboard into senior medical affairs leadership in India and beyond.
Associate Manager - Manufacturing Quality Assurance (Upstream)
Pfizer
Visakhapatnam5+ Years · Onsite25 SeptThis Associate Manager - MQA Upstream role at Pfizer’s Vizag sterile manufacturing site is a critical quality leadership position supporting cGMP compliance across solution/emulsion preparation, vial and ampoule washing, depyrogenation, filling, capping, and collection. The position safeguards patient safety and product quality for Pfizer’s sterile injectable portfolio, where regulatory scrutiny from USFDA, MHRA, and TGA is intense. By reviewing electronic batch records, assessing AMPS exceptions, overseeing alarm and trend reports, and investigating deviations, the MQA professional ensures every batch meets Pfizer standards and global regulatory expectations. This is a compelling opportunity for experienced QA professionals to deepen expertise in sterile manufacturing, electronic batch systems, and inspection readiness while influencing shop-floor quality culture, process simplification, and continuous improvement at one of Pfizer’s key India sites.
Associate Manager – Manufacturing Quality Assurance
Pfizer
Visakhapatnam5+ Years · Onsite25 SeptPfizer’s Associate Manager, Manufacturing Quality Assurance, based in Visakhapatnam, is a critical cGMP compliance role supporting terminal sterilization, visual inspection and packaging operations. The position ensures that manufacturing processes, batch records and equipment systems remain inspection-ready for global regulators such as USFDA, MHRA and TGA. This is not a generic QA job: it directly protects patient safety, product quality and Pfizer’s commercial supply continuity. The role offers a strong platform for experienced pharma QA professionals to deepen expertise in sterile operations, electronic batch record review, deviation/AMP impact assessment and audit management. With Pfizer’s science- and risk-based quality culture, the successful candidate gains exposure to advanced manufacturing systems, cross-functional troubleshooting and process simplification, making it an excellent long-term career move within global pharmaceutical operations.
Site Engagement Liaison
ICON
Mumbai5+ Years · Hybrid25 SeptSite Engagement Liaison responsible for fostering relationships with clinical trial sites, supporting complete site management, and contributing to clinical research activities in a sponsor-dedicated model. The role requires extensive onsite monitoring and clinical trial management experience and involves approximately 60% travel.
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Speciality Care Advisor (field based in Pune)
Bristol Myers Squibb
Pune5+ Years · Remote25 SeptField-based pharmaceutical commercial role focused on territory sales, customer and account mapping, healthcare professional engagement, scientific activities and hospital formulary inclusion.
Medical Advisor Head Office - Mumbai
Boehringer Ingelheim
Mumbai5+ Years · Onsite25 SeptMedical Affairs role focused on scientific engagement, therapeutic-area insights, medical projects, KOL development, medico-marketing strategy, product registration support and medical labeling activities.
Manager QA - EPD Quality Systems
Abbott
Mumbai5+ Years · Onsite25 SeptManager QA – EPD Quality Systems responsible for managing Quality Systems related initiatives within the EPD Quality System organization to ensure safe, effective and quality products.
Area Manager
Lupin
Ahmedabad5+ Years · Onsite25 SeptManage regional sales operations, drive primary and secondary sales targets, and lead a team of medical representatives in Ahmedabad.
Quality Operations Specialist
Novartis
Hyderabad5+ Years · Hybrid25 SeptNovartis is seeking a Specialist, Quality Operations in Hyderabad to safeguard GxP conformity across its pharmaceutical quality management system. This role sits at the intersection of compliance, change control, audit readiness, and continuous improvement, directly supporting the delivery of safe, effective medicines. By managing change controls, GxP documentation, and quality KPIs, the specialist helps prevent compliance risks that could delay regulatory approvals or commercial supply. The position offers a compelling opportunity to work within a global healthcare leader, partner with cross-functional stakeholders, and deepen expertise in Novartis Quality Management Systems. For quality professionals seeking broad exposure to audits, investigations, and operational excellence, this role provides a strong platform for career progression in Hyderabad’s thriving life-sciences hub.
Senior Data Scientist – Surfaceome Biology
Amgen
Hyderabad5+ Years · Hybrid25 SeptAmgen's Bioinformatics Technologies group, part of the ARIA (Automation, Research Data Systems, Informatics, and AI) organization, is building the computational foundation for next-generation targeted and multispecific therapeutics. This Senior Data Scientist – Surfaceome Biology role sits at the precise intersection of AI/ML engineering and cell-surface biology, where systematic characterization of the surfaceome drives antigen discovery, protein density quantification, and internalization modelling. For a computational biologist based in India, this is a rare opportunity to work inside a global pharma discovery engine rather than a service vendor, shaping atlases and predictive models that directly nominate therapeutic candidates. The position delivers deep exposure to multi-omics integration, generative modelling, agentic AI and translational validation design, with a clear pathway into principal scientist or computational discovery leadership tracks.
Scientist, Biomarker Analysis
Amgen
Hyderabad5+ Years · Onsite25 SeptAmgen's Scientist, Biomarker Analysis role in Hyderabad is a strategic addition to the Global Development - Precision Medicine organization, specifically within Computational Biology and Translational Analytics. As Amgen expands its India innovation footprint, this position will deliver high-quality clinical biomarker analytics across oncology, inflammation, rare disease, cardiovascular/metabolic, and obesity programs. The scientist will transform complex multi-omics, imaging, and clinical trial data into actionable translational insights that inform target engagement, patient stratification, mechanism validation, and benefit-risk decisions. This is a compelling opportunity for a quantitative biologist to work at the interface of drug development, advanced statistics, and responsible AI, influencing global portfolio decisions while helping build a high-impact precision medicine capability at Amgen India. The role offers deep scientific ownership, cross-functional collaboration, and exposure to late-stage clinical programs.
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.
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.
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.