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Hiring | Drug Safety Physician | Life Sciences Qualification: MBBS/MD Location : PAN India Experience : 8+ Years Budget : Upto 35 LPA Relevant experience in Clinical Safety, Pharmacovigilance, Drug Safety, or Clinical Research Key Responsibilities - Conduct medical review and scientific evaluation of safety data and literature. - Perform signal detection, validation, assessment, and contribute to signal management activities. - Author and review aggregate safety reports, including DSURs, PBRERs, Risk Management Plans (RMPs), and Drug Safety Reports (DSRs). - Review Clinical Study Reports (CSRs), Individual Case Safety Reports (ICSRs), and provide expert medical input on safety-related matters. - Ensure compliance with global regulatory guidelines and pharmacovigilance processes. - Collaborate with cross-functional teams, support audits, and provide medical guidance to stakeholders. - Contribute to process improvements, scientific discussions, and strategic safety initiatives. Preferred Skills - Strong knowledge of Pharmacovigilance, Clinical Safety, and Regulatory Affairs - Experience in Signal Management and Aggregate Report Authoring - Excellent scientific writing, analytical, and problem-solving skills - Solid communication and stakeholder management abilities If you meet the above criteria or know someone who would be a great fit, feel free to share your updated resume at gaurangna@latinumhr.com & jobs@ats.latinumhr.com .