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

• Strong 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 [email protected] & [email protected]

📌 Drug Safety Physician (Telangana)
🏢 Latinum Hr Solutions
📍 Telangana