01Overview
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 .
