Full-Time Medical Reviewer I

• Review and approve post-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports.
• Perform medical/causality assessment, coding, and assess seriousness.
• Determine listedness/expectedness and company causality.
• Write company comments, follow-up questions, and analyze similar events.
• Review literature screening search strategy and articles for ICSRs/SAEs.
• Review database outputs and provide input in Periodic/Development Safety Update Reports.
• Participate in signal detection activities and write reports.
• Propose action for possible signals.
• Writing PV Procedures
• Mentoring less experienced Physicians

• Medically qualified as a physician with demonstrated experience in Pharmacovigilance.
• Experience in aggregate reports and signal detection desirable.
• Excellent interpersonal skills.
• Ability to plan, organize, prioritize, and execute multiple tasks.
• Effective cross-cultural and cross-functional teamwork.
• Strong communication and presentation skills.

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