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 176–200 of 249 jobs
Director, Process Development- Drug Product
Amgen
Hyderabad5+ Years · Onsite24 SeptLead and build the Drug Product Technologies organization at Amgen Hyderabad, driving process development, digital transformation, and global biotech deliverables.
Medical Governance Lead
Novartis
India5+ Years · Onsite24 SeptMedical Governance Lead accountable for strengthening governance, compliance, SOP adherence, MLR oversight, audit readiness and Managed Access Program governance across Medical Affairs activities in India.
Head of Manufacturing and Supply Services Hyderabad Hub
Sanofi
Hyderabad5+ Years · Hybrid23 SeptLead and direct large-scale manufacturing and supply operations and teams (400+ personnel) at the Hyderabad Hub.
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Speciality Care Advisor - Cardiology (field based in Mumbai)
Bristol Myers Squibb
Mumbai5+ Years · Onsite23 SeptDrive territory performance for Cardiology by identifying and mapping healthcare accounts, engaging healthcare professionals, supporting scientific activities and executing commercial strategies in line with BMS objectives and values.
Director, Process Development - Drug Product
Amgen
Hyderabad5+ Years · Onsite23 SeptLead the establishment and growth of Amgen's Drug Product Technologies organization in Hyderabad, building a high-performing team and operating model while expanding global drug product process-development capabilities through technical, digital and cross-functional innovation.
Associate Manager SRC Governance
Sanofi
Hyderabad5+ Years · Hybrid22 SeptOur Team: Sanofi Business Operations (SBO) is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. Main responsibilities: Committee review Governance team support to set up governance to review meetings for all 4 committee reviews for ESRs, Phase 1 studies, Global Health Studies and MRPTC as per the established operating model. Study Review Committee (SRC) Primary responsibility is to Set up governance to review approval meetings for all 4 committee reviews - Company Sponsored Studies & Externally Sponsored Collaborations (CSS & ESC), ISS, Global Health Studies as per the established operating model. Identify stakeholders, organize pre-SRC meetings, maintain Action Registers, and manage audit readiness. Medico-Regulatory Pharmacovigilance Transversal Committee (MRPTC) Lead the conduct of the MRPTC including preparatory meetings, minutes, follow-up, and stakeholder coordination. Phase I SRC Set up governance for Phase 1 study review approval meetings, ensure cross-functional alignment, and manage risks and timelines.
Medical Affairs Manager
Johnson & Johnson
Mumbai5+ Years · Hybrid22 SeptMedical Affairs leadership role supporting DePuy Synthes country strategy, evidence generation, stakeholder engagement, innovation and medical/scientific activities.
Regional Manager - Coronary & Renal Denervation
Medtronic
Hyderabad5+ Years · Remote22 SeptLead and coach a regional sales team to drive commercial growth and market adoption of advanced coronary and cardiovascular medical technologies at Medtronic.
Manager Regulatory Affairs
Abbott
Mumbai5+ Years · Onsite22 SeptExperienced Regulatory Affairs professional responsible for product registration submissions, regulatory strategy, agency interactions, lifecycle management, and regulatory support for established pharmaceutical products.
Director, Global Clinical Trial Services, India
Regeneron
Hyderabad5+ Years · Onsite22 SeptDirector-level clinical operations leadership role responsible for clinical trial delivery across India, from feasibility through site close. The position leads India-based teams and FSP partners while coordinating with global functional leaders, sites, investigators, vendors, and regulatory authorities.
Regulatory Labeling Mgr
Amgen
Hyderabad5+ Years · Onsite21 SeptSupport the planning, coordination, and execution of EU and global labelling compliance activities within the Regulatory Affairs organisation.
Senior Clinical Trial Manager (Sr. CTM) - Internal Medicine
Thermo Fisher Scientific
Mumbai5+ Years · Remote21 SeptSenior Clinical Trial Manager responsible for end-to-end clinical trial start-up and clinical deliverables for moderate-to-high complexity studies across Internal Medicine and related therapeutic areas.
Clinical Trial Vendor Manager
Lupin
Pune5+ Years · Onsite21 SeptSenior clinical research role responsible for selecting, contracting, overseeing, and governing external vendors supporting clinical trials. The position focuses on quality, timelines, budgets, regulatory compliance, GCP standards, and vendor performance.
Sr MSL - Heart Health
Bayer
Delhi NCR5+ Years · Hybrid20 SeptDrive scientific engagement and education with key thought leaders as a Senior Medical Science Liaison specializing in Heart Health at Bayer.
Manager - EM Demand & Distribution Planner
Sun Pharmaceutical Industries Ltd
Mumbai5+ Years · Onsite20 SeptThe Manager - EM Demand & Distribution Planner leads demand forecasting, inventory planning, distribution coordination, S&OP participation, and supply-chain performance improvement for assigned pharmaceutical portfolios. The role combines strategic forecasting with monthly operational planning and cross-functional collaboration.
Clinical Data Coordinator - Senior
ICON
Bangalore5+ Years · Hybrid19 SeptSenior Clinical Data Coordinator supporting sponsor-dedicated clinical research programmes through clinical data management planning, discrepancy resolution, cross-functional collaboration, study documentation, data reconciliation, coding, cleaning, and mentoring of junior coordinators.
Senior Specialist Submission Management
Merck
Bangalore5+ Years · Onsite19 SeptSenior regulatory submission management role focused on planning, publishing, quality checking and dispatching regulatory submissions to Health Authorities.
Manager, Medical Writing FSP
Thermo Fisher Scientific
Remote5+ Years · Remote19 SeptManager, Medical Writing FSP leading Medical Writers, resource planning, clinical document delivery, quality review, regulatory writing, training, and client-facing Medical Writing activities within a global clinical research organization.
Lead Clinical Data Science Programmer
ICON
Bangalore5+ Years · Hybrid18 SeptLead the design, development and validation of clinical data science programming solutions for complex clinical trials. Provide technical leadership, ensure data quality and integrity, collaborate across clinical functions, and mentor junior programmers.
Manager, Clinical Operations
Syneos Health
Hyderabad5+ Years · Hybrid18 SeptManage and provide operational leadership to Clinical Operations staff across study startup, site activities, monitoring and close-out. Oversee people, quality, regulatory compliance, resourcing, metrics and project delivery while supporting customer requirements and operational planning.
Quality Specialist (QMS, Documentation)
Merck
Bangalore5+ Years · Onsite18 SeptQuality Assurance Specialist responsible for QMS management, audits, investigations, quality documentation, regulatory compliance, staff training, quality metrics, and continuous improvement within Merck's Life Science division in India.
Manager CMC Regulatory Affairs
Regeneron
Hyderabad5+ Years · Hybrid18 SeptManager-level CMC Regulatory Affairs role supporting global clinical regulatory submissions, CMC compliance, investigational product release, cross-functional coordination, and team leadership in Hyderabad.
Quality Continuous Improvement (CI) Partner, Greater Asia (GA)
Becton, Dickinson and Company (BD)
Multiple Locations (APAC)5+ Years · Remote18 SeptAdvanced Quality individual contributor role focused on Quality training, capability building, coaching, Continuous Improvement, and Quality Excellence across BD's Greater Asia organization. The position combines regulated Quality expertise with facilitation, investigation, root cause analysis, and continuous improvement capabilities.
Quality Engineering, QA Expert, Commissioning & Qualification Audit and Inspection Support
Lonza
Hyderabad5+ Years · Hybrid18 SeptQA Expert role providing Global Quality Engineering oversight for commissioning and qualification, CAPEX projects, audits, inspections, remediation, CAPA, and cGMP compliance.
SME Packing
Sun Pharmaceutical Industries Ltd
Mumbai5+ Years · Onsite17 SeptTechnical subject-matter expert responsible for pharmaceutical packing machinery across Sun Pharma sites, driving equipment performance, troubleshooting, compliance, OEE improvement, automation upgrades and operational excellence.