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 76–100 of 117 jobs
Associate - IC Plan Design
Amgen
Hyderabad2-5 Years · Onsite24 SeptDesign, model, and execute field incentive compensation plans and sales contests at Amgen Hyderabad.
Research Associate : Pharma Analytical
Lupin
Pune2-5 Years · Onsite24 SeptDrive analytical data management, software validation, and enterprise application implementation for R&D operations at Lupin Pune.
Medical Data Reviewer
ICON
Bangalore2-5 Years · Remote23 SeptProvide expert medical oversight of clinical trial data, ensuring accuracy, consistency, and patient safety in a sponsor-dedicated model.
Clinical Data Coordinator II (CDC II)
ICON
Bangalore2-5 Years · Hybrid23 SeptDeliver high-quality clinical data management tasks, maintaining eCRFs, data validation specifications, and supporting study metrics.
Clinical Document Agent (2nd Shift - 2 PM to 11 PM IST)
Syneos Health
Remote2-5 Years · Remote23 SeptCreate and manage clinical project documentation, subject files and electronic documentation while converting raw study data into electronic formats and ensuring compliance with established clinical procedures and quality requirements.
Associate- Quality Complaints
Amgen
Hyderabad2-5 Years · Onsite23 SeptManage assigned product complaint records and investigation activities within Amgen's global quality complaint process, ensuring procedural compliance, record quality, timely closure and continuous improvement.
Sr Professional Quality Management
Syneos Health
Hyderabad2-5 Years · Hybrid22 SeptSr Professional Quality Management Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. Job Responsibilities Job Summary Performs various activities (analysis, investigation, reporting, administration) related to ‘GXP’ (e.g. Good Clinical Practice or Good Pharmacovigilance Practice) and related topics for Clinical departments (therapeutic areas and functions).
Executive - Regulatory Affairs
Sun Pharmaceutical Industries Ltd
Panoli2-5 Years · Onsite22 SeptSupport plant and corporate Regulatory Affairs activities for global pharmaceutical submissions, GMP documentation and QMS coordination, with a focus on accurate compilation, review and timely execution of regulatory deliverables.
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.
Senior Healthcare Executive
Pfizer
Chennai2-5 Years · Onsite22 SeptField-based healthcare sales role responsible for achieving territory sales targets, customer engagement, product promotion, market intelligence, and compliant execution of Pfizer commercial activities.
Study Grant Analyst II
Parexel
Hyderabad2-5 Years · Remote21 SeptStudy Grant Analyst II responsible for developing and analyzing clinical study grants for Phase I-IV trials, supporting pre-sales proposals and awarded projects, and ensuring compliance with fair market value and healthcare regulations.
Global Executive Assistant Capability Support Specialist
Sanofi
Hyderabad2-5 Years · Onsite21 SeptProvides high-level administrative, coordination, and talent acquisition support to Sanofi's Global Executive Development and Global Capability teams. The role focuses on executive calendar management, travel, meetings, purchasing, vendor coordination, communications, and confidential information handling.
Specialist Quality Assurance Auditor – Innovative Medicine
Johnson & Johnson
Mumbai2-5 Years · Onsite21 SeptQuality Assurance specialist focused on R&D and Pharmacovigilance auditing, regulatory inspection support, GxP compliance, and quality systems. The role requires hands-on PV experience and supports audits across global healthcare operations.
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.
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.
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.
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.
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.
Regulatory AI & Automation Specialist
Roche
Hyderabad2-5 Years · Onsite17 SeptDrive hands-on AI, machine learning, document intelligence, and workflow automation for global regulatory operations, improving regulatory document processing, submission dossier management, compliance tracking, and operational efficiency.
District Manager, Oncology - Srinagar
Johnson & Johnson
Srinagar2-5 Years · Onsite17 SeptDistrict Manager responsible for driving oncology business growth in the Srinagar territory through sales execution, healthcare professional engagement, territory planning, scientific communication, and customer relationship management.
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.
Safety & PV Specialist I - Literature Case processing
Syneos Health
Delhi NCR2-5 Years · Onsite15 SeptPharmacovigilance role focused on literature case processing, ICSR handling, safety database activities, MedDRA coding, quality review and regulatory safety reporting.