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 1–25 of 43 jobs
Analyst Customer Facing Effectiveness
Sanofi
Hyderabad2-5 Years · OnsiteYesterdaySanofi is hiring an Analyst Customer Facing Effectiveness in Hyderabad to support commercial operations through incentive plan analysis, sales target allocation, and sales force effectiveness tracking. The role sits within the global Go-to-Market Capabilities team and requires analytical skills and commercial operations experience.
Statistical Programmer
Sanofi
Hyderabad2-5 Years · Onsite4 days agoSanofi is hiring a Statistical Programmer in Hyderabad to support Medical Affairs biostatistics within Sanofi Business Operations. The role centres on building QC'd statistical outputs — tables, figures and listings — for publications and ad-hoc analyses, using SAS and CDISC standards.
Central Clinical Research Associate
Sanofi
Hyderabad2-5 Years · Onsite6 days agoSanofi is hiring a Central Clinical Research Associate in Hyderabad to support rare disease registry studies. The role coordinates with principal investigators and site staff and covers start-up, monitoring, data review and site-management tasks under ICH-GCP.
R&D Scientific Competitive Intelligence Analyst
Sanofi
Hyderabad2-5 Years · Onsite20 days agoSanofi is recruiting an R&D Scientific Competitive Intelligence Analyst for its Hyderabad offshore hub, where patent data is used to map competitor innovation and shape R&D portfolio choices. The position sits in the Competitive Intelligence group of the Global R&D Strategy and Portfolio Management team.
Global QMS Manager
Novartis
Hyderabad2-5 Years · Hybrid27 days agoNovartis is hiring a Global QMS Manager in Hyderabad to oversee compliance and governance of Batch Release Hub configurations and related quality systems. The role works across Quality, IT and business teams on system changes, validation, documentation and global user support.
Associate, Membership – Contracts & Pricing Execution
Amgen
Hyderabad2-5 Years · Onsite7 OctAmgen is hiring an Associate, Membership – Contracts & Pricing Execution in Hyderabad. The role supports U.S. pharmaceutical membership operations covering customer eligibility, contract alignment, pricing-related processes, customer setup, data maintenance, and compliance activities.
Manager – Standards Medical Writer (Biomedical Data Stewardship)
Amgen
Hyderabad2-5 Years · Onsite5 OctAmgen is expanding its global Biomedical Data Stewardship (BMDS) capabilities in India, and this Manager, Standards Medical Writer role sits at the intersection of medical writing, clinical data standards, and regulatory governance. Based in Hyderabad, the position supports Amgen's Center for Design & Analysis by advancing protocol standards, structured authoring, and metadata repository (MDR) execution. The role is critical to ensuring protocols are fit-for-purpose, inspection-ready, and aligned with global clinical development strategy across therapeutic areas. By partnering with Global Regulatory Writing, Clinical Development, Regulatory, and TA SMEs, the writer-manager helps harmonize protocol language, govern libraries, and improve data quality from authoring through submission. This is a compelling opportunity for life-sciences professionals seeking global cross-functional exposure, influence over enterprise standards, and a career path in medical writing, clinical data governance, or regulatory operations within a top-tier biopharma.
Scientific Writer - Health Economics and Value Assessment (HEVA)
Sanofi
Hyderabad2-5 Years · Onsite1 OctSanofi’s Global Hub in Hyderabad is a strategic engine for medical, HEVA, and commercial excellence. As a Scientific Writer – Health Economics and Value Assessment (HEVA), you will translate complex health economic and value evidence into clear, compliant publications and communication tools. This role is pivotal for demonstrating product value to payers, healthcare professionals, and internal stakeholders, directly supporting access and reimbursement decisions across Specialty Care, Vaccines, General Medicines, and CHC. You will partner with global HEVA, RWE, and scientific communication teams, managing deliverables from manuscripts and abstracts to Core Value Decks. This is an outstanding opportunity to build therapeutic area expertise, influence global value narratives, and grow within a world-class pharmaceutical organization committed to innovation and patient impact.
Mgr, Regulatory Consulting (Office based)
Syneos Health
Hyderabad2-5 Years · Hybrid1 OctManager, Regulatory Consulting leads regulatory consulting projects, regulatory submissions, client engagements, project teams, and people-management activities while providing strategic and operational regulatory advice across pharmaceutical and related product development programs.
Scientific Writer HEVA
Sanofi
Hyderabad2-5 Years · Onsite1 OctScientific Writer – Health Economics and Value Assessment (HEVA) develops high-quality HEVA communications and evidence-based content supporting product value, access, and reimbursement decisions across global business units.
Central Monitor Senior Associate
Amgen
Hyderabad2-5 Years · Onsite1 OctCentral Monitor Senior Associate independently performs proactive, data-driven central monitoring across clinical studies, using analytics and structured review to detect risks affecting patient safety, data quality, and protocol adherence.
Associate Project Specialist - Medical Communications
Sanofi
Hyderabad2-5 Years · Onsite30 SeptThis Associate Project Specialist – Medical Communications role at Sanofi in Hyderabad sits within Sanofi Business Operations (SBO), a centralized hub supporting Specialty Care, Vaccines, General Medicines, Consumer Healthcare, and R&D. The position is pivotal to delivering high-quality scientific publications and medical education materials—slide decks, abstracts, posters, and manuscripts—that communicate Sanofi’s clinical evidence to healthcare professionals, regulators, and payers. By coordinating project timelines, compliance submissions, budgets, and stakeholder communication, the specialist ensures scientific writers can focus on content excellence. This is an exceptional opportunity for life-sciences graduates to gain end-to-end exposure to medical publications, publication management tools like iEnvision and PromoMats, and global medical affairs operations. It offers a launchpad into medical writing, publications management, or scientific communications leadership within a top-tier pharmaceutical company.
Associate Quality Complaints
Amgen
Hyderabad2-5 Years · Onsite30 SeptOwn and execute quality complaint activities across the global complaint process, ensuring compliant handling, accurate records, timely closure, and appropriate escalation. The role connects customer feedback with quality processes and continuous improvement.
- B
Clinical Trial Support Specialist
Bristol Myers Squibb
Hyderabad2-5 Years · Onsite30 SeptSupport end-to-end clinical trial submission operations by preparing submission-ready documents, maintaining clinical trial systems and data, coordinating regulatory milestones, and enabling efficient clinical development activities across the oncology portfolio.
Specialist, Quality Services – Product Complaints
Sanofi
Hyderabad2-5 Years · Onsite29 SeptSanofi's Global Manufacturing & Supply Services hub in Hyderabad is the operational backbone of the company's worldwide product quality agenda, and this Specialist Quality Services (Product Complaints) position sits at the frontline of post-market surveillance. The role owns intake, triage, categorization and closure of Product Technical Complaints across medical devices, pharmaceuticals, biologics and combination products — a workflow that directly protects patient safety and feeds the investigation, field alert and pharmacovigilance machinery of a 110,000-person life-sciences leader. Because Sanofi is investing heavily in AI-driven data standards and reusable quality data, specialists here gain exposure to modern QMS tooling and global cross-functional stakeholders. For an early-career quality professional, it is an exceptional launchpad: high regulatory visibility, structured GxP discipline and a clear route into broader quality, compliance and pharmacovigilance careers.
- B
Scientific Writer II
Bristol Myers Squibb
Hyderabad2-5 Years · Onsite29 SeptScientific Writer II responsible for authoring and coordinating regulatory and clinical documents, integrating scientific, medical, and regulatory input while managing document strategy, review cycles, timelines, quality, and compliance.
Clinical Monitoring (CM)
Syneos Health
Hyderabad2-5 Years · Hybrid29 SeptSupport clinical trial oversight through independent monitoring, patient-level data review, study and site-level trend analysis, risk identification, and risk-based quality management.
- B
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.
Site Start Up EUCTR II
Parexel
Hyderabad2-5 Years · Hybrid26 SeptSupport complex clinical trial initiation, focusing on EU CTR compliance and CTIS database management.
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.
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.
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.
- B
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.
Associate - IC Plan Design
Amgen
Hyderabad2-5 Years · Onsite24 SeptDesign, model, and execute field incentive compensation plans and sales contests at Amgen Hyderabad.