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 51–75 of 160 jobs
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 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.
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.
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.
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.
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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.
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.
Manager, Clinical Operations
Syneos Health
Hyderabad5+ Years · Hybrid29 SeptLead clinical operations teams at Syneos Health in Hyderabad, overseeing site activations, monitoring, and regulatory submissions.
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.
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.
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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.