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 26–50 of 108 jobs
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.
Senior Data Scientist – Surfaceome Biology
Amgen
Hyderabad5+ Years · Onsite6 OctAmgen is hiring a Senior Data Scientist – Surfaceome Biology in Hyderabad to develop computational and AI/ML approaches for integrating biomedical data and supporting target discovery, validation, biomarker development, and therapeutic research.
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.
Clinical Data QC Reviewer
Sanofi
Hyderabad5+ Years · Onsite4 OctThis Clinical Data QC Reviewer role at Sanofi Business Operations in Hyderabad sits at the heart of clinical data integrity for registry and real-world evidence studies. As Sanofi centralizes global medical, HEVA, and commercial support, this position ensures eCRF, EDC, and SAS listings meet rigorous quality control standards before they inform regulatory submissions, publications, or safety decisions. The reviewer will work with Medidata RAVE and cross-functional stakeholders to validate data, manage issues, perform UAT, and uphold GCP, FDA, EMA, and ICH expectations. It is a compelling opportunity for experienced clinical data professionals to deepen therapeutic and systems expertise, contribute to Sanofi’s Specialty Care, Vaccines, and General Medicines pipeline, and influence process improvements in a global, science-driven environment.
Medical Science Liaison
Bayer
Hyderabad0-2 Years · Onsite4 OctMedical Science Liaison role focused on scientific exchange, medical education and engagement with healthcare professionals, thought leaders, medical societies and advisory boards within an assigned therapeutic area.
Director, Global Clinical Trial Services, India
Regeneron
Hyderabad5+ Years · Onsite4 OctSenior operational leadership role responsible for clinical trial delivery across India, from feasibility through site close, while ensuring compliant execution, strong vendor performance, effective resource planning, and alignment with global clinical development standards.
Senior Scientific Writer – Health Economics and Value Assessment (HEVA)
Sanofi
Hyderabad5+ Years · Onsite2 OctSenior scientific writing role focused on Health Economics and Value Assessment communications. The position develops high-quality HEVA evidence communications and supports global access, reimbursement and scientific communication strategies across Sanofi.
Group Lead - Scientific Writing
Sanofi
Hyderabad5+ Years · Onsite2 OctLeads a multi-layered scientific writing organization supporting pharmaceutical and healthcare content across therapeutic areas. Drives scientific quality, publication and medical education deliverables, stakeholder engagement, technology adoption and operational efficiency.
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Negotiation Governance Lead, Site Contracting
Bristol Myers Squibb
Hyderabad5+ Years · Onsite2 OctLead complex clinical trial site contract and budget negotiations, governance, escalations and process improvements for BMS-sponsored research. The role provides strategic oversight, negotiation expertise, training and quality governance across global clinical contracting operations.
Artwork Reviewer - Global Artwork
Amgen
Hyderabad0-2 Years · Onsite2 OctArtwork Reviewer responsible for reviewing pharmaceutical product artworks, templates, supplier print proofs, and partner-generated artwork while ensuring compliance with Amgen procedures and quality requirements.
Clinical Development Scientist
Novartis
Hyderabad0-2 Years · Onsite2 OctClinical Development Scientist / Clinical Scientific Expert I supporting global clinical trials through clinical data review, scientific insight generation, data quality oversight, study documentation, and cross-functional trial activities. The role contributes to delivering clinical study outcomes within schedule, budget, quality, compliance and performance standards.
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.
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.
Regulatory AI & Content Specialist
Roche
Hyderabad5+ Years · Onsite30 SeptThis Regulatory AI & Content Specialist role at Roche India sits within Product Development Regulatory and Roche Services & Solutions, a strategic hub driving digital transformation of regulatory content. The position bridges regulatory affairs, structured content management, and generative AI, helping standardize reusable content for AI-powered authoring and automation. It is critical to Roche’s global submissions because high-quality, compliant regulatory documents accelerate approvals and support patient access. The specialist configures templates and metadata within Roche’s in-house GenAI platform, supports document authors, and ensures outputs are submission-ready. For regulatory professionals, this is a rare chance to combine ICH-CTD expertise with AI-enabled authoring, gaining future-facing skills in regulatory operations and platform governance while contributing to medicines that reach millions.
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.
Project Manager – Medical Communications
Sanofi
Hyderabad5+ Years · Onsite30 SeptThis Project Manager – Medical Communications role at Sanofi Business Operations, Hyderabad, is a strategic enabler of scientific publication and medical education delivery across global therapeutic areas. As part of Scientific Communications Operations, the position coordinates publication planning, medical events, advisory boards, compliance submissions, and vendor budgets for slide decks, abstracts, posters, and manuscripts. It sits at the intersection of medical affairs, medical writing, and operational excellence, ensuring Sanofi's scientific narrative reaches healthcare professionals, regulators, and payers with accuracy and timeliness. The role is compelling because it combines project leadership, people mentoring, and cross-functional global stakeholder management within a top-tier biopharma. It also offers exposure to AI/GenAI-enabled workflows, ServiceNow ESM, iEnvision, PromoMats, and publication compliance tools—skills highly valued across India's growing medical communications and medical affairs hubs.
Director, Commercial Analytics - Obesity
Amgen
Hyderabad5+ Years · Onsite30 SeptLead global commercial analytics for Amgen's obesity business, driving strategy, sales execution, and U.S. market intelligence from Hyderabad.
Manager Biostatistics (Study Statistician and/or Study Lead Statistician)
Amgen
Hyderabad5+ Years · Onsite30 SeptProvide statistical expertise, lead clinical study analyses, and drive tech-enabled transformation in biostatistics at Amgen Hyderabad.
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.
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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.
Manager, Scientific Communications
Amgen
Hyderabad5+ Years · Onsite29 SeptManager-level Scientific Communications role within Amgen's Global Medical Organization, responsible for developing scientific and medical content, publications, medical information materials, and communication strategies across global audiences and therapeutic areas.
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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.
Expert Scientific Writer
Sanofi
Hyderabad5+ Years · Onsite28 SeptSanofi Business Operations in Hyderabad is seeking an Expert Scientific Writer to drive high-impact medical and publication content for Specialty Care, Vaccines, General Medicines and R&D portfolios. This role is central to Sanofi's global scientific communication strategy, ensuring accurate, compliant and compelling publication materials that inform healthcare professionals and support product lifecycle decisions. The writer will manage end-to-end development of abstracts, posters, manuscripts, slide decks and medical education assets in PromoMats/iEnvision, while coaching junior writers and partnering with medical, HEVA and commercial teams. For an experienced medical writing professional, this is a rare opportunity to shape therapeutic-area narratives, maintain Good Publication Practice standards and influence how Sanofi's clinical evidence reaches global stakeholders.