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 76–100 of 251 jobs
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 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.
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.
Senior Clinical Research Associate II
Pfizer
Mumbai5+ Years · Onsite1 OctLead and support moderately complex clinical research projects, overseeing study startup, monitoring plans, regulatory activities, budgets, drug supply, and site-level execution for pharmaceutical clinical studies.
Access Field Manager
Novartis
Delhi NCR5+ Years · Onsite30 SeptThis Access Field Manager role at Novartis is a strategic market-access position focused on Delhi and surrounding states/UTs. It sits at the intersection of public health, government affairs, payer engagement and commercial strategy, ensuring that innovative Novartis therapies are included in state formularies and reach reimbursed beneficiaries through sustainable health-system solutions. The position is critical as India's healthcare access landscape becomes more decentralised, with state governments, public health bodies and payers shaping adoption pathways. By co-creating MoUs, disease awareness programmes, protocol shaping and alternative funding models, the Access Field Manager directly influences patient access and Novartis's long-term portfolio performance. This is a compelling opportunity for experienced healthcare strategy professionals who want to shape policy, build high-level partnerships and translate access barriers into measurable patient impact across Delhi's evolving health ecosystem.
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.
Associate Manager – Automation Engineering
Pfizer
Visakhapatnam5+ Years · Onsite30 SeptPfizer’s Vizag manufacturing site is a critical node in the company’s global supply chain, producing medicines that reach patients worldwide. The Associate Manager – Automation role sits at the heart of this operation, ensuring that Emerson DeltaV DCS, PI Historian, and field instrumentation systems run reliably, safely, and in full compliance with GMP. This position is not just about maintaining equipment; it directly enables uninterrupted production of life-saving therapies. By joining Pfizer’s forward-thinking engineering team, you will work on complex automation projects, drive digital transformation, and collaborate with cross-functional experts. The role offers a compelling career opportunity for engineers seeking to deepen their expertise in pharmaceutical automation, validation, and compliance within a world-class organization.
Manager, Operational Excellence (Lean Six Sigma)
Pfizer
Visakhapatnam5+ Years · Onsite30 SeptThe Manager, Operational Excellence at Pfizer's Vizag manufacturing campus sits at the intersection of Lean Six Sigma methodology, GMP compliance and enterprise-wide continuous improvement. Operating inside Pfizer's Integrated Manufacturing Excellence (IMEx) framework, this role deploys the company's global operating system across a high-volume, regulated production site, converting shop-floor data into measurable performance gains. Because Vizag also supports translation and dossier execution documentation, the position directly influences inspection readiness and the speed at which Pfizer files and launches products in global markets. For a certified Black Belt, this is a rare opportunity to own programme governance, coach cross-functional teams and build capability at scale, with high visibility to senior leadership across manufacturing, quality, regulatory affairs and supply chain.
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.
Manager - Regulatory Affairs
Abbott
Mumbai5+ Years · Onsite30 SeptManage Regulatory CMC activities for assigned products, including registrations, submissions, lifecycle compliance, regulatory strategy, health-agency interaction and cross-functional coordination within Abbott's Established Pharmaceutical Products division.
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.
Associate Manager - Quality Investigations
Pfizer
Vizag5+ Years · Onsite29 SeptPfizer’s Vizag manufacturing site is a critical node in the company’s global supply chain, producing medicines that reach patients worldwide. The Associate Manager – Investigation role sits at the heart of quality assurance and compliance, ensuring that deviations, out-of-specification results, and atypical events are thoroughly examined and resolved. This position directly supports Pfizer’s quality culture, which is science- and risk-based, flexible, and patient-focused. By identifying root causes and implementing robust corrective and preventive actions, the incumbent protects product safety, regulatory standing, and supply continuity. For professionals with a pharma quality background, this is a compelling opportunity to work with a global leader, gain exposure to complex investigations, and develop expertise that is highly valued across the industry. The role offers visibility with cross-functional teams and regulatory inspections.
Associate Manager - Reliability Engineering
Pfizer
Visakhapatnam5+ Years · Onsite29 SeptPfizer’s Vizag manufacturing site is a critical node in the company’s global sterile injectables and pharmaceutical supply network. The Associate Manager – Reliability Engineering plays a central role in safeguarding asset uptime, calibration compliance, and cGMP readiness across utilities, buildings, and production equipment. This position is not just maintenance—it is a strategic enabler of uninterrupted medicine supply. By driving reliability-centered maintenance, root cause failure analysis, and predictive maintenance optimization, the role directly supports Pfizer’s mission to deliver breakthroughs to patients. For experienced engineering professionals, this is a compelling opportunity to work at the intersection of advanced manufacturing, quality systems, and regulatory compliance, with exposure to aseptic processing and process automation. Career growth is strong, and the impact on patient outcomes is tangible.
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.
District Manager - Neuroscience - Kolkata
Johnson & Johnson
Kolkata5+ Years · Onsite29 SeptDistrict Manager responsible for pharmaceutical sales growth across an assigned neuroscience territory, with a focus on psychiatry, healthcare-professional engagement, KOL development, distributor management and execution of scientific and commercial strategies.
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.
Clinical Project Manager - FSP
Thermo Fisher Scientific
Mumbai5+ Years · Remote29 SeptClinical Project Manager responsible for end-to-end delivery of clinical research projects, serving as the primary sponsor contact and leading cross-functional teams across quality, time, cost, risk, financial stewardship, and vendor oversight.
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
Parexel
Bangalore5+ Years · Onsite29 SeptManager, Clinical Operations responsible for team oversight, clinical project delivery, resource planning, staff development, quality control, client management, and compliance with clinical research standards and regulations.