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 101–125 of 249 jobs
Manager, Clinical Operations
Syneos Health
Hyderabad5+ Years · Hybrid29 SeptLead clinical operations teams at Syneos Health in Hyderabad, overseeing site activations, monitoring, and regulatory submissions.
Quality Specialist (QMS, Documentation)
Merck KGaA
Bangalore5+ Years · Onsite29 SeptQuality Assurance Specialist responsible for managing QMS, quality documentation, audits, investigations, compliance, and continuous improvement within Merck's Life Science division in India.
Regional Manager, IC
Boston Scientific
Chandigarh5+ Years · Onsite29 SeptDrive interventional cardiology sales and lead regional teams at Boston Scientific in Chandigarh and New Delhi.
Principal Clinical Programmer (Rave EDC)
Syneos Health
Remote5+ Years · Remote29 SeptSenior clinical programming leadership role focused on Rave EDC programming, custom functions, clinical database development, technical support, study oversight, quality review, and program-level leadership across multiple clinical studies.
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.
Safety Operations Advisor 1
Novo Nordisk
Bangalore5+ Years · Onsite28 SeptProvide medical expertise across global pharmacovigilance operations by evaluating adverse events, performing medical reviews and causality assessments, ensuring regulatory reporting compliance, and driving consistent safety practices across clinical and post-marketing programs.
Zonal Business Manager - South - Lung Cancer
Johnson & Johnson
Bangalore5+ Years · Onsite28 SeptDrive business growth in the assigned South territory for the Oncology franchise, maintaining effective customer relations and maximizing sales objectives.
Sr. Territory Manager, Eyecare
AbbVie
Indore5+ Years · Remote28 SeptDrive eyecare sales performance, brand KPIs, and customer relationships across the Indore territory for AbbVie.
Manager, Medical Writing FSP
Thermo Fisher Scientific
Remote5+ Years · Remote28 SeptLead Medical Writing operations by managing writers, allocating resources, overseeing clinical and regulatory deliverables, maintaining quality and compliance, supporting proposals and business development, and developing team training programs.
Associate Manager Quality Control
Pfizer
Vizag5+ Years · Onsite28 SeptEnsure the delivery of safe and effective products through rigorous quality control, method validations, and risk-based 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.
Business Unit Director – Cardiovascular, Renal & Metabolism (CVM)
AstraZeneca
Mumbai5+ Years · Hybrid27 SeptThis Business Unit Director – CVM role at AstraZeneca India puts the successful candidate at the helm of one of the company's most strategically critical therapeutic franchises: Cardiovascular, Renal and Metabolism. India carries an enormous and fast-rising burden of hypertension, heart failure, diabetes and chronic kidney disease, making CVM a core growth pillar alongside oncology and respiratory. The director owns full P&L accountability, shapes brand strategy across the portfolio, leads a large field force, and partners with Medical, Market Access and Regulatory to widen patient access. Because the position reports into senior India commercial leadership and interfaces with global brand teams, it offers exceptional visibility, influence over launch and lifecycle decisions, and a genuine platform for shaping patient outcomes at population scale.
Regulatory Consultant (CMC-EU, GCC & AU)
Syneos Health
Remote5+ Years · Remote27 SeptLead CMC regulatory authoring, lifecycle management, and global submissions across EU, GCC, and AU markets.
Medical Advisor
Pfizer
Mumbai5+ Years · Onsite27 SeptProvide scientific and medical expertise for Specialty Care and Internal Medicine pipeline products, support medical strategy and launch readiness, generate evidence, engage healthcare professionals, and ensure compliant execution of Medical Affairs activities.
Medical Advisor – Specialty Care & Internal Medicine
Pfizer
Mumbai5+ Years · Onsite27 SeptPfizer's Medical Advisor role in Mumbai sits at the heart of the company's Specialty Care and Internal Medicine medical strategy, bridging global scientific evidence with Indian clinical practice. As Pfizer expands its pipeline across oncology, vaccines and internal medicine, this position ensures that launch readiness, real-world evidence generation and healthcare professional engagement are executed with uncompromising scientific integrity. The advisor acts as the credible scientific voice of the organisation — informing formulary decisions, shaping medical education and translating complex trial data into practical clinical insight. For physicians holding an MD with Medical Affairs experience, this is a high-visibility platform to influence patient outcomes at scale, work alongside cross-functional commercial, regulatory and clinical leaders, and build the therapeutic-area depth that defines senior medical affairs careers in India's fast-growing pharmaceutical sector.
Shift Manager - Manufacturing Suite
Pfizer
Vizag5+ Years · Onsite26 SeptThis Shift Manager – Suite 1 role at Pfizer’s Vizag manufacturing site is central to ensuring uninterrupted supply of critical medicines. You will lead a production suite, balancing people, technology, and financial resources to meet cGMP, quality, and delivery targets. The position directly supports Pfizer’s mission by safeguarding batch compliance, investigating deviations, and driving continuous improvement. For pharma professionals with manufacturing and people leadership experience, this is a high-impact opportunity to influence site performance, develop teams, and work with advanced pharmaceutical technologies. Vizag is a key Pfizer manufacturing hub, offering exposure to global quality standards and cross-functional collaboration. The role suits results-driven leaders who thrive in regulated environments and want to grow into senior operations or quality leadership.
Senior Clinical Research Associate II
Pfizer
Mumbai5+ Years · Onsite26 SeptPfizer's Research & Development division in Mumbai is recruiting a Senior Clinical Research Associate II to own the operational delivery of clinical trials across India. This is a high-visibility, site-facing role at the intersection of science, regulation and execution: the CRA II protects patient safety, data integrity and protocol compliance while keeping complex studies on time and on budget. Because Pfizer's Indian sites increasingly contribute to global Phase I–III programmes, this position directly shapes how quickly new therapies move from protocol to regulatory submission. For a life-sciences professional with GCP depth and sponsor-side monitoring experience, the role offers structured mentoring responsibilities, budget and drug-supply ownership, and exposure to inspection readiness at a global scale — a genuine springboard into Clinical Trial Lead and Clinical Program Manager careers.
Manager Regulatory Affairs - Delhi
Boehringer Ingelheim
Delhi NCR5+ Years · Onsite26 SeptRegulatory Affairs Manager responsible for product registrations, regulatory submissions, approvals, renewals, CMC changes and regulatory intelligence for assigned therapeutic areas in India.
Assistant Manager, Clinical Data Management
Teva Pharmaceuticals
Bangalore5+ Years · Onsite26 SeptAssistant Manager responsible for leading and supporting Clinical Data Management activities, ensuring accurate and timely study delivery, quality compliance, process improvement and effective stakeholder coordination.
Director, Global Clinical Trial Services, India
Regeneron
Hyderabad5+ Years · Onsite26 SeptDirector responsible for operational leadership of clinical trial delivery in India, from feasibility through site close, while building local capabilities and ensuring compliant execution aligned with global clinical development standards.
Sr. Territory Manager, Eyecare
AbbVie
Hyderabad5+ Years · Remote26 SeptSenior commercial pharmaceutical role focused on eyecare territory performance, customer engagement, brand objectives, market intelligence and strategic sales execution.
Greenfield Account Lead
Medtronic
Delhi NCR5+ Years · Remote26 SeptManage strategic healthcare accounts, build executive-level customer relationships, and drive business growth through account planning and portfolio expansion.
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Senior Manager, Clinical Operations Manager
Bristol Myers Squibb
Mumbai5+ Years · Onsite26 SeptSenior management role overseeing clinical operations staff and country-level clinical trial execution, resources, performance and compliance.
Senior Clinical Database Designer
Iqvia
Kochi5+ Years · Onsite26 SeptIQVIA is the world's largest clinical research organisation, and its Kochi delivery centre supports hundreds of global trials across oncology, cardiology, vaccines and rare disease. The Senior Clinical Database Designer owns the technical backbone of a study's data capture: interpreting the protocol, designing the electronic case report form (eCRF), writing edit specifications and configuring the InForm EDC environment so that clean, submission-ready data reaches sponsors on time. Because every downstream deliverable — statistical analysis, regulatory submission, safety reporting — depends on the database being built correctly the first time, this is a high-visibility, high-accountability position. It suits a detail-obsessed clinical data professional who wants to deepen EDC and technical design expertise inside a global CRO, with structured exposure to ICH-GCP, CDISC-adjacent standards and sponsor-facing collaboration.
Manager, Scientific Writing
Novartis
Hyderabad5+ Years · Onsite26 SeptThis Manager, Scientific Writing role at Novartis sits within Studio Operations, a critical hub for scientifically accurate, MLR-compliant promotional and medico-marketing content. The position shapes how brand and product stories are communicated across digital, print, and omnichannel assets while reflecting the latest ISI, PI, and label changes. As Novartis advances its innovative medicine portfolio, this leader ensures that every newsletter, iCVA, brochure, and social post is both engaging and regulatory-ready. The opportunity is compelling for experienced scientific writers who want to influence global content strategy, mentor junior talent, and collaborate across India, US, Ireland, and Mexico. It offers a rare blend of scientific depth, commercial impact, and compliance rigour within a top-tier pharmaceutical organisation.