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 1–25 of 83 jobs
Medical Director, Patient Safety Physician
AstraZeneca
Bengaluru5+ Years · HybridTodayAstraZeneca's Medical Director, Patient Safety Physician role places a medically qualified safety leader at the centre of benefit-risk decision-making for high-impact therapies spanning late-stage development through post-marketing. Based in Bengaluru, the position owns the clinical safety strategy for assigned programmes, defining identified and potential risks, setting safety go/no-go criteria, and shaping risk-minimisation approaches that ultimately influence labelling and regulatory outcomes. Because AstraZeneca's pipeline stretches across oncology, cardiovascular, respiratory and rare disease, this is a rare opportunity to work on genuinely transformative medicines while collaborating with regulators, QPPVs and external partners. For physicians seeking to move beyond bedside practice into strategic pharmacovigilance leadership, it offers exceptional visibility, cross-cultural exposure and durable long-term career capital.
Team Lead – Global Regulatory Affairs Labelling Strategist
Sanofi
Hyderabad5+ Years · HybridTodaySanofi's Global Regulatory Affairs (GRA) labelling organization is the function that shapes the Company Core Data Sheet (CCDS), US Prescribing Information, EU SmPC and patient leaflets that govern how every Sanofi medicine is described to physicians, regulators and patients worldwide. As Team Lead GRA Labelling Strategist in Hyderabad, the incumbent owns both a portfolio of products and a team of labelling strategists, converting clinical study reports, pharmacovigilance signals and competitive intelligence into approved labelling text. The role sits at the crossroads of regulatory strategy, drug safety and medical affairs, making it one of the most visible scientific-commercial positions in the company. Because labelling decisions directly unlock new indications, line extensions and marketing authorizations across the US, EU and WHO markets, this position offers exceptional exposure to senior executive governance and long-term career capital.
Associate Global Development Scientist Director I
AstraZeneca
Bangalore5+ Years · HybridYesterdayAstraZeneca is recruiting a senior clinical development scientist for its Bangalore site. The role supports late-phase clinical programmes across protocol work, data and safety review, publications and regulatory documents in a hybrid team setting.
Senior Manager - Publications Delivery Lead - Scientific Publications (GBS BBU)
AstraZeneca
Bengaluru5+ Years · HybridYesterdayAstraZeneca is recruiting a Publications Delivery Lead to set up and run a multi-tier scientific publications team staffed by content authors, visual designers and iEnvision specialists. The role pairs people leadership with operational governance, covering SOPs, delivery metrics, quality control and global collaborator management.
Senior Analyst, Enterprise Competitive Intelligence
Novartis
Hyderabad5+ Years · Hybrid3 days agoNovartis is hiring a Senior Analyst, Enterprise Competitive Intelligence in Hyderabad on a hybrid basis. The role involves competitive intelligence analysis across brands, franchises and therapy areas, supporting clinical, commercial and regulatory strategy discussions.
Statistical Science Director
AstraZeneca
Bengaluru5+ Years · Hybrid5 days agoAstraZeneca is hiring a Statistical Science Director in Bengaluru to lead statistical strategy across global medicine development, from early discovery through registration. The role owns statistical content for study designs, protocols, analysis plans and submissions, and represents statistical strategy at internal governance forums.
Team Lead - Global Regulatory Affairs Labeling Strategist
Sanofi
Hyderabad5+ Years · Hybrid6 days agoThis senior leadership position sits within Sanofi's Global Regulatory Affairs Labeling (GRAL) function in Hyderabad, shaping the corporate core data sheets (CCDS), US Prescribing Information, EU SmPC and WHO labeling that govern how Sanofi's medicines are described worldwide. Labeling strategy is the final gatekeeper of a medicine's approved claims — every safety signal, new indication or line extension must be translated into defensible regulatory text. As Team Lead, you will chair multidisciplinary labeling working groups, defend proposals before the Labeling Governance Committee, and represent Sanofi in Health Authority negotiations across EU and US procedures. Because labeling decisions directly unlock or restrict commercial claims, this role enjoys exceptional visibility with senior executive management and offers a rare blend of scientific depth, cross-functional influence and people leadership inside one of the world's largest pharmaceutical companies.
Commercial Insights Manager
AstraZeneca
Mumbai5+ Years · Hybrid8 days agoAstraZeneca's Insights Manager role sits at the commercial heart of one of the world's most science-led biopharmaceutical companies, translating complex market, customer and brand data into decisions that shape how medicines reach patients across India. Based at the Mumbai Commerz hub, the position partners directly with Business Unit, Marketing and Sales leadership, converting IQVIA, Veeva CRM, sales and digital engagement signals into forecasts, segmentation strategies and field-force plans. For analytics professionals who want their models to influence real commercial strategy rather than sit unused in a slide deck, this is a rare opportunity to apply AI, GenAI and cloud analytics inside a global pharma enterprise. The role also offers enterprise-scale visibility, as solutions piloted locally are scaled across AstraZeneca's international commercial network, keeping patient outcomes at the centre of every recommendation.
Direct Materials Life Cycle Manager
Novartis
Hyderabad5+ Years · Hybrid9 days agoNovartis is hiring a Direct Materials Life Cycle Manager in Hyderabad to lead supplier introduction and direct materials projects for the Small Molecules platform. The job focuses on excipients and chemicals, project delivery, and compliance with quality, regulatory and GMP requirements.
Senior Manager – Commercial Forecasting & Analytics
Amgen
Hyderabad5+ Years · Hybrid10 days agoAmgen is recruiting a Senior Manager for Commercial Forecasting & Analytics in Hyderabad to lead forecasting work for global and U.S. commercial teams. The position combines individual forecasting work with team oversight and cross-regional collaboration.
Senior Clinical Programmer II
AstraZeneca
Bengaluru5+ Years · Hybrid15 days agoAt AstraZeneca, the Senior Clinical Programmer II role sits within the Biometrics and Clinical Data Sciences function, powering the data-driven oversight of global trials in cardiovascular, renal, metabolic, respiratory, and immunology. This position is pivotal to turning complex clinical data into validated listings, dashboards, and actionable insights that accelerate trial decisions, improve data quality, and support regulatory submission readiness. The programmer partners with data management, clinical operations, biometrics, and study teams to build scalable programming solutions using SAS, Python, R, SQL, Power BI, and Spotfire. As an individual contributor and mentor, you will shape enterprise standards, reduce cycle times, and ensure inspection-ready outputs. This is a compelling career opportunity for an experienced clinical programmer who wants to blend deep technical mastery with patient-focused drug development at a top global pharmaceutical company.
Director, Patient Safety
AstraZeneca
Bengaluru5+ Years · Hybrid23 days agoAt AstraZeneca, the Director-Patient Safety role in Bangalore is a strategic leadership position within Global Patient Safety. It directly influences how innovative medicines progress from early development through lifecycle management while protecting patients and maintaining regulatory trust. This opportunity matters because patient safety is central to benefit-risk decision-making, signal evaluation, and inspection readiness across AstraZeneca's oncology, respiratory, cardiovascular, and specialty pipelines. The director will lead a regional group, connect safety enablement with cross-functional partners, and shape safety strategy in a global environment. For experienced pharmacovigilance professionals, this is a compelling chance to combine scientific rigor, people leadership, digital innovation, and external regulatory engagement. It offers high visibility, responsibility for compliance and process improvement, and the ability to accelerate safe access to transformative therapies worldwide.
Revenue Manager
ICON
Chennai5+ Years · Hybrid7 OctICON is hiring a Revenue Manager in Chennai to oversee revenue management and financial reporting for clinical trial projects. The role focuses on revenue recognition, invoicing, financial forecasting, project performance analysis, and financial controls.
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.
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.
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.
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.