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You will be updated with latest job alerts via emailQualification :Bachelors or Masters 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.
Full Time