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Full-Time Opportunity: This is a permanent, full-time position with a competitive package and real career growth potential.
Job Description
When our values align, there's no limit to what we can achieve.
Key Requirements:
MBBS or MD from a recognized medical school2+ years of experience in ICSR medical reviewGood understanding of medical terminologyExperience in pharmacovigilance, drug safety, or clinical practiceBasic 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 guidelinesMaintaining an awareness of global regulatory requirements, reporting obligations and organizing workload to ensure compliance with internal and regulatory timelines for adverse event reportingCommunicating and discussing issues related to review process with Line Manager/ Proje...