Pharma, Clinical Research & Healthcare Jobs in India
512 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 326–350 of 423 jobs
CRA I - FSP
Thermo Fisher Scientific
Mumbai0-2 Years · Remote21 SeptClinical Research Associate I role supporting clinical trial monitoring and site management in a fully remote position, with responsibility for protocol compliance, data quality, site relationships, documentation and audit readiness.
Centralized Monitoring Analyst (Level I & II)
Thermo Fisher Scientific
Bangalore2-5 Years · Hybrid21 SeptCentralized Monitoring Analyst role supporting clinical trials through analysis of operational and patient data, identification of trends and risks, documentation of findings and centralized monitoring activities.
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.
Associate I– Reg CMC Strategy (LEC Team)
Pfizer
Chennai0-2 Years · Onsite19 SeptAssociate I supporting Regulatory CMC Strategy activities for Legal Entity Change variations across global markets, including regulatory assessments, document coordination, CMC authoring, submission planning, and regulatory database activities.
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, RA Publishing & Submissions
Astellas
Bangalore2-5 Years · Onsite19 SeptManager-level Regulatory Affairs Publishing & Submissions role focused on global regulatory submissions, publishing operations, submission standards, quality control and regulatory operations.
Safety Surveillance Adviser I
Novo Nordisk Global Business Services (GBS)
Bangalore2-5 Years · Onsite19 SeptSafety Surveillance Adviser I supporting Global Patient Safety activities across the lifecycle of Novo Nordisk medicines, including safety surveillance, signal and aggregate management, safety labelling, regulatory safety reporting, and cross-functional safety communication.
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.
Sr. Officer - QC
Sun Pharma Laboratories Ltd
Jammu0-2 Years · Onsite19 SeptQuality Control role responsible for pharmaceutical sample analysis, analytical method activities, laboratory documentation, instrument monitoring and participation in quality investigations at Sun Pharma's Jammu facility.
Associate I – Reg CMC Strategy (LEC Team)
Pfizer
Chennai0-2 Years · Onsite19 SeptSupport Regulatory CMC Strategy activities for Legal Entity Change variations across US, EU and ROW markets, coordinating global regulatory inputs, authoring impacted Module 3 sections and maintaining submission timelines under manager supervision.
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.
Associate, Medicaid – Contracts & Pricing Execution (AIN)
Amgen
Hyderabad2-5 Years · Onsite18 SeptSupport U.S. Medicaid rebate operations within Amgen's Contracts & Pricing Execution function. Execute invoice, claim, validation, dispute, payment-package, reconciliation and documentation activities while maintaining compliance, controls and audit readiness.
Senior CDA/ Clin Data Assoc II
Thermo Fisher Scientific
Bangalore2-5 Years · Hybrid18 SeptSenior Clinical Data Associate role supporting clinical data cleaning, database activities, query management, data review, study-specific processes, reporting, and training within a global clinical research organization.
Senior Clinical Research Associate II
Pfizer
Mumbai2-5 Years · Onsite18 SeptSenior Clinical Research Associate II responsible for leading moderately complex clinical research activities, study startup and monitoring planning, regulatory and ethics coordination, clinical trial budgets, drug supply, and site-level study execution.
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.
Pharmacovigilance Reporting Associate
ICON
Bangalore2-5 Years · Hybrid17 SeptPrepare and review accurate, timely pharmacovigilance safety reports for clinical trials and post-marketing activities while ensuring regulatory compliance and effective cross-functional collaboration.
Principal Clinical Programmer (Rave Programming)
Syneos Health
Remote5+ Years · Remote17 SeptLead complex Rave programming and clinical programming activities across multiple studies, providing technical expertise, quality oversight, project leadership and mentorship within clinical data management and clinical solutions.
Seniorr Associate Regulatory Writing
Amgen
Hyderabad2-5 Years · Onsite17 SeptIndependently author and manage routine to moderately complex regulatory documents while coordinating reviews, ensuring scientific accuracy, inspection readiness and timely delivery across cross-functional teams.