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 292 jobs
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.
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.
Consultant – Anesthesiologist
Asian Institute of Medical Sciences
India5+ Years · Onsite28 SeptLead clinical anesthesia services, ensure patient safety during surgical procedures, and mentor junior medical staff at AIMS.
Manager - Inpatient Services
MGM Healthcare
Chennai5+ Years · Onsite28 SeptOversee daily inpatient department operations, optimize bed management, and ensure exceptional patient service delivery in Chennai.
Senior Consultant Orthopaedics
Fortis Hospital
Delhi NCR5+ Years · Onsite28 SeptLead orthopedic patient care, complex surgeries, and advanced joint replacement procedures at Fortis Flt. Lt. Rajan Dhall Hospital.
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.
Nursing In-Charge - Emergency
Manipal Hospitals
Bangalore5+ Years · Onsite26 SeptNursing In-Charge for the Emergency Department responsible for overseeing daily operations, managing nursing staff, and ensuring compliance with clinical protocols.
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.