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Key Requirements:
MBBS or MD from a recognized medical school 2+ years of experience in ICSR medical review Good understanding of medical terminology Experience in pharmacovigilance, drug safety, or clinical practice Basic clinical training (internship/residency completed) Key Accountabilities:
General:
Maintaining a good working knowledge of the Adverse event/Safety profile of assigned products, labeling documents, data handling conventions, client’s guidelines and procedures, and global drug safety regulations and guidelines Maintaining an awareness of global regulatory requirements, reporting obligations and organizing workload to ensure compliance with internal and regulatory timelines for adverse event reporting Communicating and discussing issues related to review process with Line...