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 26–50 of 159 jobs
Senior Manager - ADaM Standards Lead (Biomedical Data Stewardship)
Amgen
Hyderabad5+ Years · Onsite17 days agoAmgen seeks a Senior Manager - ADaM Standards Lead for its Biomedical Data Stewardship team in Hyderabad. The role combines ADaM and CDISC standards leadership with people management and cross-functional work across R&D.
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.
Qualification & Validation Expert, Report Issuance
Sanofi
Hyderabad5+ Years · Onsite23 days agoSanofi is hiring a Qualification & Validation Expert for its Report Issuance team in Hyderabad, part of Global Manufacturing & Supply Services. The role involves writing and reviewing qualification documentation for facilities, utilities and equipment, and keeping that documentation compliant with global Quality requirements.
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.
Program Manager – Medical
Sanofi
Hyderabad5+ Years · Onsite28 days agoSanofi is looking for a Program Manager – Medical at its Business Operations hub in Hyderabad to lead medical affairs programme delivery across therapeutic areas. The role carries ownership of governance, budgets, risk, reporting and the supervision of associate project managers.
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Senior Manager I, FP&A (NS/EB)
Bristol Myers Squibb
Hyderabad5+ Years · Onsite7 OctBristol Myers Squibb is hiring a Senior Manager I, FP&A (NS/EB) in Hyderabad to lead financial planning and analysis activities supporting market-focused Revenue teams. The role combines revenue forecasting, budgeting, financial modelling, process improvement, stakeholder management and team leadership.
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.
Transition Manager Quality
Lonza
Hyderabad5+ Years · Hybrid6 OctLonza is hiring a Transition Manager Quality in Hyderabad to lead the transfer and improvement of Quality processes into its Global Capability Center. The role requires extensive BioPharma, pharmaceutical manufacturing, or CDMO experience with hands-on GMP-regulated Quality experience.
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Manager I, Commercialization FP&A
Bristol Myers Squibb
Hyderabad5+ Years · Hybrid6 OctThe Manager I, Commercialization FP&A role supports financial planning and operational process management for BMS commercialization activities. The position focuses on forecasting, budgeting, management reporting, process improvement, governance, relationship management and business risk oversight.
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.
Sr. Specialist LCoE Operations
Regeneron
Hyderabad5+ Years · Hybrid6 OctRegeneron is hiring a Senior Specialist Learning Center of Excellence Operations in Hyderabad to support regional training, onboarding and learning delivery for its India Global Capabilities Center. The role involves training content development, facilitation, Learning Management System administration, onboarding coordination and collaboration with regional and global stakeholders.
Quality Expert, Data Analytics and Statistical Support
Lonza
Hyderabad5+ Years · Hybrid5 OctLonza is hiring a Quality Expert for Data Analytics and Statistical Support in Hyderabad to oversee manufacturing consistency and compliance through statistical analysis. The role involves managing control charting, supporting root-cause investigations, and generating reports for Periodic Quality Review and Continued Process Verification.
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.
Global Regulatory Affairs Labelling Group Lead
Sanofi
Hyderabad5+ Years · Hybrid5 OctThis Global Regulatory Affairs (GRA) Labelling Group Lead role at Sanofi in Hyderabad is a senior people-leadership and labeling strategy position within one of the world’s leading biopharmaceutical companies. It owns the end-to-end creation, maintenance, and negotiation of corporate labeling documents—CCDS, US Prescribing Information, EU SmPC, WHO labeling, and patient leaflets—across a large portfolio of marketed, lifecycle-management, and development products. The position is pivotal to Sanofi’s ability to secure and maintain marketing authorizations, respond to health authority queries, and deliver compliant, competitive labels that support patient safety and commercial success. For experienced regulatory professionals, this is a rare opportunity to shape global labeling strategy, lead multidisciplinary teams, and influence senior governance committees while working in a hybrid, high-impact environment.
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.
Senior Global Regulatory Affairs Labeling Specialist
Sanofi
Hyderabad5+ Years · Hybrid4 OctThis Senior GRA Labeling Specialist role at Sanofi in Hyderabad is a strategic regulatory affairs position responsible for shaping corporate labeling documents such as CCDS, USPI, and EU SmPC across marketed and lifecycle products. Labeling is the final, legally binding communication of a medicine's benefit-risk profile, directly impacting patient safety and commercial viability. The incumbent will chair multidisciplinary labeling working groups, lead agency negotiations, and ensure alignment with global regulatory strategy. As Sanofi advances its pipeline in immunology, oncology, rare diseases, and vaccines, this role offers a high-visibility opportunity to influence product approvals, lifecycle extensions, and competitive differentiation. Working in a hybrid model, the specialist will collaborate with global pharmacovigilance, medical affairs, and legal teams, making it an ideal next step for an experienced labeling professional seeking global impact.
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 Manager Medical Review
Regeneron
Hyderabad5+ Years · Hybrid3 OctLead medical review and case-quality activities for global pharmacovigilance programs in a hybrid Hyderabad role, ensuring safety cases are scientifically sound, compliant, and inspection-ready.
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.
Clinical Evaluation Medical Writer
Medtronic
Hyderabad5+ Years · Hybrid2 OctClinical Evaluation Medical Writer responsible for developing and maintaining clinical evaluation and regulatory documents that support the safety, performance, reliability, and regulatory compliance of medical devices.
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.