Qualification :Bachelor's or Master’s degree in Medical
Job Responsibilities :
Reviewing and analyzing adverse event reports, clinical trial data, and other safety
information related to drugs.
• Identifying and assessing safety risks associated with drugs, and making recommendations
for managing or mitigating those risks.
• Communicating safety information to regulatory agencies, healthcare professionals, and the
general public.
• Collaborating with other members of the drug development team, including pharmacologists,
toxicologists, and statisticians, to ensure that safety issues are adequately addressed.
• Participating in the development of risk management plans, which outline strategies for
minimizing the risk of adverse events associated with drugs.
• Reviewing and approving of protocol for clinical trial safety and contributing to the report of clinical trial safety.