Pharma, Clinical Research & Healthcare Jobs in India

Senior Associate, Central Monitor, Data Surveillance, Clinical Data Sciences

Pfizer

Pfizer 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.

Quality Analyst Trainee

Desirous

A full-time Quality Analyst Trainee opening based in Chennai for candidates with zero to one year of experience. The role focuses on examining laboratory data, documenting testing protocols, and supporting quality control initiatives.

Regulatory Affairs – Executive / Trainee

Axxelent Pharma Science Private Limited

Axxelent Pharma Science Private Limited is recruiting entry-level candidates for a Regulatory Affairs Executive / Trainee position based in Tharamani, Chennai. The role involves preparing dossier packages, formatting CTD / eCTD documents, and handling regulatory compliance workflows.

Sr. Associate, Basic Results Author

Pfizer

Pfizer 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.

Revenue Manager

ICON

ICON is hiring a Revenue Manager in Chennai to oversee revenue management and financial reporting for clinical trial projects. The role focuses on revenue recognition, invoicing, financial forecasting, project performance analysis, and financial controls.

Full Stack Engineer – Biologics Discovery Platform

AstraZeneca

AstraZeneca's Global Capability Centre in Chennai is hiring a Full Stack Engineer to build the Augmented Biologics Discovery Platform — a cloud-native product suite that shortens the path from antibody idea to clinical candidate. Sitting at the intersection of software engineering, AI/ML and computational biology, the role translates complex scientific workflows into production-grade services and data products that discovery scientists use every day. This is a strategic build-out for AstraZeneca: biologics represent a fast-growing share of its oncology, respiratory and rare-disease pipeline, and the speed at which computational teams can model, rank and validate antibody candidates directly influences how quickly programmes reach IND. For engineers who want their code to shape real therapeutic programmes rather than generic enterprise software, it is a rare opportunity to work beside scientists, product leaders and MLOps specialists at global scale.

Associate II Reg Strategy, GRS Oncology

Pfizer

Support 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.

QA Documentation Intern – Smart Document System (SDS)

Pfizer

Pfizer's Chennai site is executing a Smart Document System (SDS) rollout that replaces paper-based laboratory logbooks and controlled forms with validated digital templates — a foundational step in the company's paperless-lab, documentation-control and data-integrity strategy. This 6–8 month internship places a science, pharmacy or engineering student directly inside that transformation, working alongside Quality, Engineering, Validation, Laboratory and Digital functions. Rather than merely shadowing, the intern owns template creation, field configuration, verification and qualification tracking for records that regulators routinely inspect. For a B.Pharm, M.Pharm, MSc or engineering graduate, this is rare early exposure to Good Documentation Practices, electronic records and GMP change control at a global pharmaceutical major — a credential that accelerates entry into QA, validation or regulatory documentation careers.

TMF Specialist (all levels)

ICON Strategic Solutions

TMF Specialist role supporting sponsor-dedicated clinical research projects through research, data collection, analysis, reporting, administrative support and workflow improvement.

Senior Healthcare Executive

Pfizer

Field-based healthcare sales role responsible for achieving territory sales targets, customer engagement, product promotion, market intelligence, and compliant execution of Pfizer commercial activities.

Associate, Associate Database Analyst, Clinical Database Management

Pfizer

Associate-level Clinical Database Management role supporting data monitoring, query management, database design, clinical data systems, documentation quality, and process improvement.

Associate I– Reg CMC Strategy (LEC Team)

Pfizer

Associate 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.

Associate I – Reg CMC Strategy (LEC Team)

Pfizer

Support 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.

Associate I-Reg CMC Strategy

Pfizer

Provide regulatory CMC strategy and documentation support for product license renewals and annual reports across global markets, with a focus on post-approval regulatory requirements.

Associate II - Reg CMC Strategy

Pfizer

Support 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.

Manager, Quality – Digital Systems

Pfizer

Own and continuously improve Veeva eQMS operations within Regulatory Quality Assurance, serving as the bridge between business stakeholders and digital quality systems. Drive GxP-compliant administration, governance, reporting, cross-functional programs, AI-enabled transformation, and quality-system modernization.

Pharmacovigilance Associate

ICON

Process 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.

HCE

Pfizer

Drive territory-level pharmaceutical sales and customer engagement while promoting Pfizer products to healthcare professionals, managing key accounts, supporting product availability, and maintaining strict compliance with company policies and procedures.

TMF Specialist (All Levels)

ICON