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 131 jobs
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.
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.
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.
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.
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.
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.
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.
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.
Engagement Analyst – External Expert Engagement Services
AstraZeneca
Bengaluru2-5 Years · Hybrid30 SeptThe Engagement Analyst role within AstraZeneca's External Expert Engagement Services (E3S) sits at the intersection of Medical Affairs, Commercial and Compliance operations. Based at Manyata Tech Park, Bangalore, this individual-contributor position governs the end-to-end lifecycle of engagements with healthcare providers and patients — advisory boards, consulting assignments and speaking programmes that shape how AstraZeneca's medicines are understood, prescribed and adopted. Because every such engagement carries transparency and anti-bribery obligations, the analyst protects AstraZeneca's licence to operate while accelerating scientific exchange. For professionals with 1–5 years of experience in regulated contracting or compliance workflows, the role offers global exposure, direct partnership with Medical Affairs, Nominated Signatories and Legal, and a clear pathway into compliance, medical affairs operations or risk management careers.
Senior Global Regulatory Scientist
ICON
Bangalore2-5 Years · Hybrid30 SeptSenior Global Regulatory Scientist responsible for leading global clinical-trial regulatory activities, submission strategy, regulatory project teams, client deliverables, and compliance across pharmaceutical clinical trials in India.
Associate II Reg Strategy, GRS Oncology
Pfizer
Chennai2-5 Years · Hybrid30 SeptSupport global regulatory strategy and lifecycle maintenance activities for oncology products, coordinating submissions, CMC Module 1 documentation, labeling, safety compliance activities, Health Authority responses, and cross-functional regulatory operations.
Medical Writer I / Medical Writer II
Parexel
Bangalore2-5 Years · Hybrid30 SeptDevelop high-quality pharmacovigilance and regulatory safety documents, conduct signal detection and assessment, synthesize scientific evidence, and support regulatory compliance across the product lifecycle.
Associate Director, Real World Data Statistics
AstraZeneca
Bengaluru5+ Years · Hybrid29 SeptAlexion, AstraZeneca's rare disease unit, is expanding its epidemiology and real-world evidence capability in Bangalore with an Associate Director I/II, Real World Data Statistics. This individual-contributor leadership role sits at the intersection of advanced biostatistics and regulatory science, converting disease registry, natural history, EMR and claims data into evidence robust enough to withstand FDA, EMA and other health authority scrutiny. The position matters because rare disease programmes depend on external data to characterise small, dispersed patient populations, support label expansions and satisfy post-market commitments. For an experienced statistician it offers unusual scope: methodological innovation in missingness, linkage and confounding control, direct exposure to health authority interactions, and mentorship of a growing RWD statistics function within a biotech-paced, patient-centred environment backed by AstraZeneca's global scale.
Clinical Programmer I / II
AstraZeneca
Bengaluru2-5 Years · Hybrid29 SeptThe Clinical Programmer I/II role at AstraZeneca's Manyata Tech Park campus in Bangalore sits at the intersection of clinical science and software engineering — the precise place where modern drug development is being reinvented. Reporting into the Biometrics and Clinical Programming function, this individual-contributor position converts raw trial data from EDC and third-party vendors into validated datasets, automated quality checks and executive-ready dashboards that study teams use to spot anomalies weeks earlier. Because AstraZeneca's pipeline spans oncology, cardiovascular, respiratory and rare disease, the programmer's output directly shapes how quickly and confidently go/no-go decisions are made. For a technically strong SAS or Python developer who wants their code to carry patient-level consequence rather than purely commercial consequence, this is a rare hybrid of engineering craft, regulatory rigour and genuine therapeutic impact.
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.
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.
Medical Science Liaison
Bayer
Delhi NCR2-5 Years · Hybrid29 SeptDrive scientific engagement and education as a Medical Science Liaison with Bayer in Delhi.
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.
Senior Statistical Programmer
AstraZeneca
Bengaluru2-5 Years · Hybrid28 SeptBased at AstraZeneca's Manyata Tech Park campus in Bangalore, the Senior Statistical Programmer I role sits within the Oncology Biometrics Programming department—a critical function that turns raw clinical trial data into regulatory-ready evidence. As part of a global team dedicated to eliminating cancer as a cause of death, you will support and lead statistical programming activities across high-priority oncology studies, from clinical study report development to regulatory submissions and commercialisation. This is a compelling opportunity for an experienced SAS programmer who wants to see their code influence filings, accelerate patient access, and shape evidence-based decisions. AstraZeneca's deep pipeline, collaborative research culture, and investment in science and technology make this a career-defining platform for professionals who combine technical rigour with a passion for improving patient outcomes.
Safety Physician (MBBS) | Pharmacovigilance Medical Review | Immediate Joiners Preferred
Syneos Health
Delhi NCR2-5 Years · Hybrid28 SeptPerform medical review and interpretation of adverse-event and aggregate safety information for investigational and marketed products, ensuring pharmacovigilance, regulatory, SOP, and project-specific compliance.
Associate Director, Statistical Programming – Oncology Biometrics
AstraZeneca
Bengaluru5+ Years · Hybrid28 SeptThe Statistical Programming Associate Director role within AstraZeneca's Oncology Biometrics unit in Bangalore is a senior leadership position at the intersection of clinical data science and regulatory strategy. Reporting to the Director of Statistical Programming, the position owns the planning, execution and delivery of statistical programming activities at project and study level — from clinical study report development to pivotal regulatory submissions and commercialisation support. Because AstraZeneca's ambition to eliminate cancer as a cause of death depends on converting complex trial data into credible, submission-ready evidence, this role directly influences filing timelines and approval outcomes. For an experienced SAS and CDISC leader, it offers rare exposure to global filings, cross-functional influence and a genuinely patient-centred scientific mission.