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
Robust 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 excellent fit, feel free to share your updated resume at &

📌 Clinical Research Physician Hyderabad (India)
🏢 Latinum Hr Solutions
📍 India