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 110 jobs
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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.
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.
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.
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.
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 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.
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.
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.
Regulatory Intelligence Senior Specialist
Lonza
Hyderabad5+ Years · Hybrid29 SeptDrive global regulatory intelligence surveillance and analysis across human and veterinary medicines, translating changing health authority requirements into actionable insights that support compliance, risk management, and Lonza's global CDMO operations.
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.
Regulatory Intelligence Senior Specialist
Lonza
Hyderabad5+ Years · Hybrid29 SeptRegulatory Intelligence Senior Specialist responsible for global regulatory surveillance, impact assessment, regulatory trend analysis, stakeholder collaboration, intelligence reporting, dashboards, and regulatory risk identification across human and veterinary medicines.