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 101–125 of 518 jobs
Associate Manager - Quality Compliance
Pfizer
Vizag5+ Years · Onsite3 OctAssociate Manager responsible for Quality Compliance, Data Integrity, Market Complaints, investigations, CAPA and quality systems within a regulated pharmaceutical manufacturing environment.
Senior Manager - Medical & Scientific Affairs
Roche
Mumbai5+ Years · Onsite3 OctLead medical strategy and scientific engagement for Roche Diagnostics India's cardiology and neurology solutions, driving evidence generation, HCP/KOL engagement, and compliant medical activities.
Expert - Regulatory Labelling Operations
Merck KGaA
Bangalore5+ Years · Onsite3 OctThe Expert - Regulatory Labelling Operations role focuses on global labeling operational excellence, process optimization, compliance tracking and continuous improvement within Regulatory Quality Safety (RQS).
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.
Medical Writer
Thermo Fisher Scientific
Remote2-5 Years · Remote3 OctMedical Writer responsible for producing high-quality clinical and scientific documents for pharmaceutical and CRO clients, supporting projects from planning through final delivery in a fully remote India role.
Assistant Manager, Clinical Data Management
Teva Pharmaceuticals
Bangalore5+ Years · Onsite2 OctLeads and supports Clinical Data Management delivery with subject matter expertise, study oversight, quality control and process improvement. The role combines technical CDM expertise with resource coordination, mentoring, standards development and audit support.
Manager – Quality
Johnson & Johnson
Mumbai5+ Years · Hybrid2 OctLeads Commercial Quality and Compliance for Johnson & Johnson MedTech Surgery in India and neighboring markets. Owns quality management systems, compliance, audits, post-market surveillance, distribution quality and continuous improvement across the commercial organization.
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.
Officer / Senior Officer – Quality Assurance (OSD)
Sun Pharmaceutical Industries Ltd
Halol2-5 Years · Onsite2 OctQuality Assurance opportunity at Sun Pharma's Halol plant focused on in-process quality assurance, batch documentation, validation, manufacturing oversight and cGMP compliance for oral solid dosage (OSD) operations.
Medical Writer II (MLR Reviewer)
Syneos Health
Delhi NCR2-5 Years · Hybrid2 OctMedical Writer II responsible for scientific writing, publication deliverables and medical-legal-regulatory review readiness. The role combines end-to-end medical writing, Veeva document management, MLR review, publication planning and cross-functional collaboration.
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.
Clinical Data Programmer II
Novotech
India2-5 Years · Hybrid2 OctDrive core clinical trial programming, database design, and data validation activities at a leading global CRO, ensuring strict compliance with GCDMP and ICH-GCP standards.
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.
Senior Regulatory Affairs Specialist
Medtronic
Hyderabad5+ Years · Hybrid2 OctSenior Regulatory Affairs Specialist responsible for regulatory strategy, submissions, regulatory information management, compliance assessments, and global product registrations. The role supports medical-device and/or pharmaceutical regulatory activities and collaborates with business and international regulatory teams.
Sr Regulatory Consultant (CMC, EU mkt) (Office based)
Syneos Health
Hyderabad5+ Years · Hybrid2 OctLead and contribute to regulatory consulting projects with a strong focus on CMC regulatory strategy, EU market requirements, post-approval variations, lifecycle management, and regulatory submissions for pharmaceutical products.
Senior Analyst – Clinical Study Data & CRO Performance Management
Gsk
Bengaluru5+ Years · Hybrid1 OctThis Senior Analyst – SD Performance role sits within GSK's Data Science and Clinical Systems function in Bengaluru, the engine room behind the company's global vaccine and specialty medicine trials. The position owns the strategic, contractual and performance-management layer of GSK's clinical outsourcing model, ensuring preferred CRO partners delivering data management and clinical systems work to benchmark quality, cost and timeline standards. Because GSK's R&D pipeline spans respiratory, immunology and inflammation, oncology, HIV and infectious diseases, reliable CRO performance directly protects trial integrity and submission timelines. For professionals with clinical research or clinical systems experience, this is a rare chance to move from hands-on execution into strategic service-delivery leadership inside a top-tier global biopharma, with visibility across global stakeholders and genuine scope to shape how GSK manages its external data-science ecosystem.
Senior Scientific Writer - HEVA
Sanofi
Hyderabad5+ Years · Hybrid1 OctSanofi, a global leader in healthcare, is seeking a Senior Scientific Writer for its Health Economics and Value Assessment (HEVA) team at the Sanofi Global Hub in Hyderabad. This role is pivotal in communicating the value of Sanofi's pharmaceutical portfolio to global stakeholders, including payers, healthcare professionals, and regulatory bodies. By creating high-impact scientific publications and HEVA communication deliverables, you will directly influence access and reimbursement decisions, ultimately ensuring patients receive life-changing therapies. This position offers a unique opportunity to work at the intersection of science, health economics, and medical communications, collaborating with cross-functional teams across R&D, Medical Affairs, and Market Access. If you are passionate about translating complex HEVA evidence into compelling narratives and want to grow your career in a dynamic, innovation-driven environment, this role at Sanofi is an exceptional platform.
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.
Pharmacist
Prashanth Group of Hospitals
Padur0-2 Years · Onsite1 OctManage hospital pharmacy operations, dispense medications accurately, and ensure strict compliance with pharmaceutical guidelines.
Assistant Clinical Project Manager
Clario
Bangalore0-2 Years · Remote1 OctSupport clinical project managers with study administration, financial tracking, cross-functional coordination, Salesforce configuration and clinical research operations while ensuring quality, compliance and timely delivery.
Medical Writing Specialist
Novo Nordisk
Bangalore5+ Years · Onsite1 OctSenior medical writing specialist role responsible for leading clinical reporting deliverables, setting direction for complex medical writing work, coordinating global stakeholders, and driving quality and process improvements across clinical development programmes.
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.