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 51–75 of 81 jobs
Clinical Trial Manager
Astellas
Bangalore2-5 Years · Hybrid22 SeptClinical Trial Manager responsible for planning, setting up, and executing assigned clinical trials while coordinating cross-functional teams, vendors, investigators, sites, budgets, timelines, and trial deliverables in compliance with GCP, ICH, SOPs, and regulatory requirements.
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.
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, 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.
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.
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.
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.
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.
Safety Surveillance Adviser I
Novo Nordisk
Bangalore2-5 Years · Onsite16 SeptSafety Surveillance Adviser role within Global Patient Safety, supporting product safety surveillance, safety labelling, aggregate reporting, risk management and proactive safety communication across the medicine lifecycle.
Sr. Mgr, Sales Training
AbbVie
Bangalore5+ Years · Hybrid16 SeptSenior sales training leader responsible for designing, delivering and sustaining training interventions for AbbVie's therapeutic business and improving field-force productivity.
Communication BP, LS India & Communications Lead, India
Merck
Bangalore5+ Years · Onsite16 SeptLead the end-to-end communications agenda for Merck's Life Science business in India, shaping brand presence, employee engagement and external communications while translating regional and global strategy into locally relevant narratives.
(Sr) Project Manager, Feasibility Site Activation
ICON
Bangalore5+ Years · Hybrid16 SeptSenior Project Manager role focused on Study Start-Up, feasibility and site activation for global clinical studies. The position owns SSU strategy and execution, regulatory and ethics pathways, site contracts, timelines, risks and cross-functional delivery.
Global Labelling Lead
ICON
Bangalore5+ Years · Remote15 SeptGlobal Labelling Lead responsible for regulatory labelling strategy, compliance, document management and cross-functional coordination for pharmaceutical or biotechnology development projects.
Director, CDM Programming
Thermo Fisher Scientific
Bangalore5+ Years · Hybrid15 SeptSenior leadership role overseeing Clinical Data Management Programming operations, people, resources and project delivery. The position drives departmental strategy, quality, compliance, client engagement and innovation within Thermo Fisher Scientific's clinical research organization.
CDM PM
Thermo Fisher Scientific
Bangalore5+ Years · Remote14 SeptLead clinical data management projects and programs from operational, quality, timeline and financial perspectives. Serve as a primary client liaison while coaching data-management teams, managing resources and budgets, mitigating project risks and ensuring delivery across clinical studies.
CDC II
ICON
Bangalore2-5 Years · Hybrid13 SeptSupport clinical data management activities for clinical trials by maintaining eCRFs and validation specifications, reconciling clinical and third-party data, monitoring study metrics and resolving data issues. The role contributes to high-quality clinical data delivery within a global clinical research organisation.
Senior CDA/ Clin Data Assoc II
Thermo Fisher Scientific
Bangalore2-5 Years · Hybrid13 SeptPerform clinical data management and data cleaning activities for clinical trials while ensuring compliance with GCP, SOPs and client requirements, with responsibility for specialized processes and support to junior staff.
Senior Specialist Submission Management
Merck Group
Bangalore5+ Years · Onsite13 SeptSenior regulatory submission management specialist responsible for planning, compiling, publishing, quality-checking, and dispatching regulatory submissions while ensuring compliance, data integrity, and submission timelines.
Sr. International RA Specialist
BD
Bangalore5+ Years · Onsite13 SeptSenior Regulatory Affairs professional responsible for supporting global medical device registrations and lifecycle activities across multiple international markets. The role combines regulatory strategy, technical documentation review, risk assessment, and cross-functional coordination to enable compliant market access.
PK Medical Writer
ICON
Bangalore2-5 Years · Remote12 SeptDevelop and deliver high-quality Clinical Pharmacology & Pharmacometrics documents, including population PK/PD plans and reports, CSRs, protocols, and regulatory clinical documents. The role supports clinical research projects through scientific writing, document coordination, quality control, and cross-functional collaboration.
Clinical Trial Specialist
Astellas
Bangalore2-5 Years · Hybrid12 SeptSupport the end-to-end operational delivery of assigned clinical trials at Astellas, working with Clinical Trial Leads, Clinical Trial Managers, sites, CROs, vendors, and global cross-functional teams. The role focuses on quality, compliance, accurate trial execution, and operational excellence.
Quality Specialist II
Teva Pharmaceuticals
Bangalore2-5 Years · Onsite12 SeptQuality Specialist II responsible for pharmaceutical quality activities including CMC documentation review, analytical method and stability documentation, equipment qualification, BMR review, and Product Quality Review/Annual Product Review activities.
Production Planning Expert
Merck KGaA
Bangalore2-5 Years · Onsite12 SeptPlanning Specialist responsible for end-to-end production planning and coordination of New Product Introduction and Development projects at the Jigani site, including ERP master data governance, resource planning, capacity coordination, and structured handovers to routine planning teams.