Pharma, Clinical Research & Healthcare Jobs in India
518 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 51–75 of 139 jobs
Senior Statistical Programmer
AstraZeneca
Bengaluru2-5 Years · Hybrid28 SeptBased at AstraZeneca's Manyata Tech Park campus in Bangalore, the Senior Statistical Programmer I role sits within the Oncology Biometrics Programming department—a critical function that turns raw clinical trial data into regulatory-ready evidence. As part of a global team dedicated to eliminating cancer as a cause of death, you will support and lead statistical programming activities across high-priority oncology studies, from clinical study report development to regulatory submissions and commercialisation. This is a compelling opportunity for an experienced SAS programmer who wants to see their code influence filings, accelerate patient access, and shape evidence-based decisions. AstraZeneca's deep pipeline, collaborative research culture, and investment in science and technology make this a career-defining platform for professionals who combine technical rigour with a passion for improving patient outcomes.
Jr. Officer - Production
Lupin
Goa2-5 Years · Onsite28 SeptManage pharmaceutical manufacturing, granulation, compression, and coating operations at Lupin in Goa.
Safety Physician (MBBS) | Pharmacovigilance Medical Review | Immediate Joiners Preferred
Syneos Health
Delhi NCR2-5 Years · Hybrid28 SeptPerform medical review and interpretation of adverse-event and aggregate safety information for investigational and marketed products, ensuring pharmacovigilance, regulatory, SOP, and project-specific compliance.
Regulatory Affairs Associate II
Teva Pharmaceuticals
Mumbai2-5 Years · Onsite28 SeptRegulatory Affairs Associate II responsible for preparing, reviewing and submitting high-quality FDA regulatory submissions, managing post-approval change controls, maintaining regulatory databases and supporting ANDA annual reports and supplements.
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Manager, RIM Governance and Engagement
Bristol Myers Squibb
Hyderabad2-5 Years · Onsite28 SeptDrive regulatory information management excellence and ensure compliance by managing health authority correspondence, queries, and regulatory workflows at Bristol Myers Squibb.
Officer - Warehouse
Lupin
Nagpur2-5 Years · Onsite28 SeptManage warehouse raw material and packaging material operations at Lupin in Nagpur.
Staff Nurse – NICU
Rainbow Children’s Medicare
Pan India2-5 Years · Onsite27 SeptProvide exceptional, specialized critical care to neonates in our state-of-the-art Neonatal Intensive Care Unit.
Site Start Up EUCTR II
Parexel
Hyderabad2-5 Years · Hybrid26 SeptSupport complex clinical trial initiation, focusing on EU CTR compliance and CTIS database management.
Medical Writer
Thermo Fisher Scientific
Remote2-5 Years · Remote26 SeptMedical Writer responsible for producing high-quality medical and scientific documents across clinical research programs. The role supports clinical study reporting, regulatory documentation, scientific communication and delivery of accurate, compliant client-ready content.
Staff Nurse - Nursing (ICU)
Shalby Limited
India2-5 Years · Onsite26 SeptProvide specialized critical care nursing, monitor critically ill ICU patients, and collaborate with multidisciplinary medical teams at Shalby Limited.
Senior Clinical Research Associate I
Pfizer
Mumbai2-5 Years · Onsite26 SeptPfizer’s Senior Clinical Research Associate I role is a pivotal site-facing position within Pfizer’s global clinical development organization. Based in Mumbai, this CRA will manage and monitor investigator sites for complex trials, often in oncology, vaccines, internal medicine or infectious diseases. The role directly protects patient safety, data integrity and regulatory compliance while accelerating enrollment, database release and close-out. As Pfizer expands its India clinical portfolio, experienced monitors who can partner with investigators, resolve site issues and uphold ICH-GCP are critical to bringing new therapies to patients. This is a compelling opportunity to deepen therapeutic expertise, work in a matrix global team and build a pathway toward clinical operations leadership, site care partnership or trial management in India’s growing life-sciences sector.
Senior Biostatistician
Iqvia
Bengaluru2-5 Years · Hybrid26 SeptThe Senior Biostatistician at IQVIA in Bengaluru is a strategic, client-facing role at the intersection of clinical trial design, regulatory-grade evidence, and advanced analytics. IQVIA supports pharmaceutical, biotechnology, and medical device sponsors across global programs, so this position directly influences how studies are powered, analyzed, and reported. The role owns statistical methods sections, analysis plans, datasets, and tables, listings, and figures (TLFs) while guiding junior staff and collaborating with data management, clinical, and programming teams. It is compelling for professionals who want to deepen expertise in CDISC, ICH-GCP, and modern trial methodology while gaining leadership exposure, budget accountability, and direct client interaction. It also offers a pathway into principal, team lead, or sponsor-side biostatistics roles in India’s rapidly expanding life-sciences market.
Senior Medical Writer
Gsk
Bengaluru2-5 Years · Onsite26 SeptGSK is a global biopharmaceutical leader focused on vaccines and specialty medicines across respiratory, immunology, oncology, HIV and infectious diseases. The Senior Medical Writer in Bengaluru sits within a high-impact R&D documentation function that translates complex clinical and regulatory data into clear, compliant submissions. This role directly supports protocols, clinical study reports, CTD modules, investigator brochures and health-authority responses, making it central to accelerating GSK's pipeline and patient access. Working in a global matrix with clinical leads, biostatisticians and asset teams, the writer ensures scientific integrity and timely delivery. For experienced medical writers, this is a compelling opportunity to deepen regulatory writing expertise, collaborate across therapeutic areas, and contribute to medicines and vaccines that impact billions. GSK's culture of ambition for patients, accountability and inclusion further makes this a strong career platform in India's fast-growing biopharma sector.
Senior Associate – Technology Transfer
Pfizer
Visakhapatnam2-5 Years · Onsite26 SeptPfizer's Vizag site is one of the company's flagship manufacturing and technology-transfer hubs, supplying sterile and solid oral products to regulated markets worldwide. The Senior Associate – Technology Transfer position sits at the intersection of technical operations, validation science and regulatory compliance, making it one of the most consequential roles in the product lifecycle: nothing moves from development to commercial scale without it. You will own the transfer of new molecules from R&D into commercial manufacturing, design and execute exhibit batches, defend process validation packages during US FDA and multi-market inspections, and troubleshoot deviations that could otherwise delay launch. For a pharma professional with 2–5 years of experience, this is a rare chance to build a global transfer portfolio with a top-tier innovator, gaining exposure to steriles, medical devices and advanced quality systems.
Maintenance Planner and Scheduler
Novartis
Hyderabad2-5 Years · Hybrid25 SeptThis Maintenance Planner and Scheduler role at Novartis in Hyderabad is critical to keeping pharmaceutical manufacturing operations compliant, reliable, and inspection-ready. The position sits at the intersection of engineering, quality assurance, and production, ensuring that calibration and maintenance activities are planned, executed, and documented in line with GMP expectations. By managing master data in SAP, COMOS, and CMX, monitoring work order backlogs, and supporting audits, the planner directly enables uninterrupted supply of medicines. For professionals with an engineering background and German language skills, this is a compelling opportunity to gain deep exposure to Novartis’s global technical operations, work on continuous improvement projects, and build a career in pharmaceutical maintenance and compliance. It offers a rare blend of hands-on scheduling, cross-functional collaboration, and strategic site reliability impact.
Area Medical Advisor - Hepatology
Gsk
Bengaluru2-5 Years · Hybrid25 SeptGSK’s Area Medical Advisor, Specialty, Hepatology is a field-facing Medical Affairs role based in Bengaluru, designed to be the scientific bridge between GSK’s hepatology portfolio and the external clinical community. You will translate complex clinical data into credible, on-label scientific exchange with Key External Experts, gastroenterologists, hepatologists and institutional stakeholders. As GSK advances specialty medicines and vaccines across respiratory, immunology, oncology, HIV and infectious diseases, hepatology remains a critical therapy area where medical evidence, real-world insights and compliant scientific engagement shape brand strategy and patient outcomes. This position offers a rare blend of clinical science, strategic influence and cross-functional leadership, ideal for a physician seeking to deepen therapeutic expertise, build KOL networks and influence the standard of care in liver disease across India.
Analyst – Tender Data Management (Market Access Analytics)
Sanofi
Hyderabad2-5 Years · Onsite25 SeptSanofi Business Operations (SBO) in Hyderabad is the group's centralised capability hub supporting Specialty Care, Vaccines, General Medicines, Consumer Healthcare, CMO and R&D functions worldwide. The Analyst – Tender Data Management sits at the intersection of commercial strategy, market access and business intelligence, safeguarding the integrity of tender data that ultimately decides public procurement wins across global markets. Tender business is a decisive revenue channel for vaccines and general medicines, so accurate pricing, volume and award-outcome intelligence directly enables patient access. Reporting into the Tender Management function, this role blends data stewardship, commercial insight and cross-border stakeholder engagement — an excellent springboard for professionals targeting market access, pricing analytics or commercial operations leadership inside a top-tier global pharmaceutical company.
Externally Sponsored Research Specialist
Sanofi
Hyderabad2-5 Years · Onsite25 SeptSanofi Business Operations (SBO) in Hyderabad seeks an Externally Sponsored Research Specialist to manage investigator-initiated and externally sponsored studies across Specialty Care, Vaccines, and General Medicines. This role is pivotal in ensuring that external research proposals align with Sanofi’s strategic priorities, comply with internal policies, and undergo rigorous scientific and financial review. By coordinating Scientific Review Committees, Fair Market Value assessments, and Clinical Trial Agreements, the specialist directly supports Sanofi’s pipeline and post-marketing commitments. This is an excellent career opportunity for clinical operations professionals to gain global exposure, work with cross-functional teams, and contribute to Sanofi’s mission of transforming patient outcomes. The position offers deep insight into medical affairs, regulatory compliance, and research governance within a top-tier pharmaceutical company.
Warehouse Associate – Pharmaceutical Manufacturing Logistics
Pfizer
Visakhapatnam2-5 Years · Onsite25 SeptPfizer's Vizag manufacturing site is one of the company's key production hubs feeding both Indian and global markets, and its warehouse function is the circulatory system of that operation. As an Assistant Associate – Warehouse, you will be the frontline custodian of raw materials, semi-finished goods and finished pharmaceuticals as they move between storage, production lines and dispatch bays. The role sits squarely inside a cGMP-regulated environment, meaning every pallet moved, every bin reconciled and every transaction logged in the computerized inventory system has a direct bearing on batch release timelines, audit outcomes and uninterrupted patient supply. For candidates with a warehousing or plant logistics background, this is a rare opportunity to build a structured pharma supply-chain career inside a global innovator, with exposure to automated high-rise storage, Microsoft Dynamics documentation and regulatory inspections.
Senior Forecasting Analyst
Novartis
Hyderabad2-5 Years · Hybrid25 SeptNovartis is seeking a Senior Forecasting Analyst to join its Strategy & Growth team in Hyderabad, supporting pipeline and lifecycle forecasts that shape commercial and investment decisions across the global portfolio. This role sits at the intersection of epidemiology, commercial strategy, and data analytics, requiring deep pharmaceutical domain knowledge and the ability to translate complex data into actionable forecasts. The successful candidate will influence board-level reviews and BD&L opportunity assessments for therapeutic areas, helping Novartis prioritize pipeline assets and optimize lifecycle management. It is an exceptional opportunity for pharma forecasting professionals to work on high-impact global products, collaborate with cross-functional leaders, and build advanced modeling capabilities using real-world and clinical trial data.
Territory Manager – Diabetes Care
Roche
Mumbai2-5 Years · Onsite25 SeptRoche Diabetes Care is a global leader in integrated diabetes management, and the Territory Manager role in Mumbai is central to ensuring its life-changing diagnostics and self-care products reach patients through robust distribution and retail channels. Reporting to the Area Sales Manager, this position combines strategic territory planning, distributor performance management, and field activation. The role directly impacts access to blood glucose monitoring, insulin delivery, and digital diabetes solutions across a competitive urban market. By translating marketing campaigns into secondary sales, managing schemes, and capturing competitor intelligence, the Territory Manager shapes Roche’s commercial footprint. For sales professionals passionate about healthcare, it offers a rare chance to work with a science-driven multinational, build deep channel partnerships, and contribute to improved diabetes outcomes while developing a long-term career in medical devices and diagnostics.
Clinical Data Team Lead
Thermo Fisher Scientific
Bangalore2-5 Years · Hybrid25 SeptLead clinical data management activities for clinical research studies, coordinating data management teams, clients, project leads, documentation, training, metrics and study deliverables.
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.
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.
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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.