Indegene Careers: Medical Reviewer & Drug Safety Physician Jobs
If you’re passionate about merging medicine and technology, Indegene careers open doors to a dynamic future in global healthcare innovation. Indegene is seeking skilled medical professionals for the role of Medical Reviewer – Pharmacovigilance (Drug Safety Physician). This position offers a unique opportunity to play a crucial role in ensuring patient safety and regulatory compliance while growing in one of the most exciting Indegene jobs in India’s healthcare industry.
Job Details:
- Job Position: Medical Reviewer – Pharmacovigilance (Drug Safety Physician)
- Location: Work from Office – Bangalore, Hyderabad, Mumbai, Pune, Delhi
(Willingness to relocate to one of these locations is mandatory)
Indegene Careers – About the Company:
Indegene is a technology-led healthcare solutions company committed to making healthcare organizations future-ready. With operations across the globe, the company combines medical expertise, advanced analytics, and innovation to deliver better patient outcomes. Indegene careers offer an environment driven by passion, collaboration, and growth, empowering professionals to work at the intersection of healthcare and technology.
Indegene Careers – Qualifications:
- MBBS and MD (mandatory)
- Valid Medical Council of India registration (mandatory)
- Strong analytical and critical-thinking skills.
- Excellent command of medical terminology, pharmacology, and disease pathology.
- High attention to detail and strong written/verbal communication.
- Team-oriented with excellent collaboration and problem-solving skills.
- Familiarity with pharmaceutical industry practices and regulatory frameworks (preferred).
Job Description:
As a Medical Reviewer – Pharmacovigilance, you will play an integral role in maintaining patient safety and compliance through detailed medical review and analysis of individual case safety reports (ICSRs). This position within Indegene careers is ideal for those seeking growth in drug safety physician careers while working in a fast-paced, global healthcare technology environment.
Key Responsibilities:
- Conduct medical review of ICSRs for accuracy, relevance, and consistency with source documentation.
- Triage and analyze adverse event reports to identify potential serious adverse events (SAEs).
- Review and validate product coding, event selection, and MedDRA coding in alignment with client and regulatory standards.
- Ensure proper classification, causality assessment, and seriousness determination for all reported events.
- Review and enhance case narratives according to client conventions and pharmacovigilance requirements.
- Provide or verify PV comments and initiate follow-ups when necessary.
- Identify and escalate safety signals or concerns in line with internal procedures.
- Maintain accuracy and completeness before final case sign-off.
- Contribute to literature surveillance and aggregate report medical review.
- Stay updated with international pharmacovigilance regulations and company SOPs.
- Collaborate with cross-functional teams to ensure scientific accuracy and compliance.
