Pharma, Clinical Research & Healthcare Jobs in India
518 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 1–6 of 6 jobs
Senior Associate, Central Monitor, Data Surveillance, Clinical Data Sciences
Pfizer
Chennai2-5 Years · Hybrid8 days agoPfizer is recruiting a Senior Associate, Central Monitor in Chennai to run risk-based monitoring of subject data in clinical trial databases. The job involves configuring and testing the RBM system at study level, defining key risk indicators and following up on signal and action resolution with global study teams.
Sr. Associate, Basic Results Author
Pfizer
Chennai2-5 Years · Hybrid7 OctPfizer is hiring a Sr. Associate, Basic Results Author in Chennai to prepare and maintain clinical trial results disclosures for public registries. The role focuses on accurate, compliant authoring and review of clinical trial results while working with cross-functional study and disclosure teams.
Associate II Reg Strategy, GRS Oncology
Pfizer
Chennai2-5 Years · Hybrid30 SeptSupport global regulatory strategy and lifecycle maintenance activities for oncology products, coordinating submissions, CMC Module 1 documentation, labeling, safety compliance activities, Health Authority responses, and cross-functional regulatory operations.
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.
Associate II - Reg CMC Strategy
Pfizer
Chennai2-5 Years · Onsite13 SeptSupport CMC regulatory strategy for global License Renewals and Annual Reports, preparing and coordinating CMC dossier contributions, applying regulatory requirements and managing submission activities under the guidance of regulatory leadership.
Pharmacovigilance Associate
ICON
Chennai2-5 Years · Hybrid10 SeptProcess and assess clinical trial and post-marketing safety cases while ensuring accurate, timely, and compliant pharmacovigilance activities. Support case intake, triage, coding, narratives, quality control, follow-up, and regulatory compliance.