
Senior Medical Risk Analyst
5 days ago
Job Overview:
The Senior Medical Safety Advisor plays a pivotal role in pharmacovigilance by providing medical expertise to evaluate safety data from various sources. This position assesses the medical and scientific relevance of serious adverse event reports within the context of the product's safety profile.
Key Responsibilities:
- Conduct medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs)
- Compose, edit, and medically review Analyses of Similar Events (AOSE) for expedited cases
- Provide coding review of AEs, SAEs, SADRs, Past medical history, Concomitant medications, or other medical data listings
- Serve as an internal consultant to pharmacovigilance case processing teams on projects being supported
Qualifications:
- Hold an MBBS OR MD degree from an accredited and internationally recognized medical school
- Have three plus (3+) years of clinical medicine practice experience after awarding the medical degree
- Have two plus (2+) years of pharmacovigilance experience
Required Skills:
- Possess sound knowledge of Medicine
- Have in-depth knowledge of applicable global, regional, and local clinical research regulatory requirements
- Be familiar with Pharmacovigilance- ICSR
This is a key role in the pharmacovigilance team requiring strong medical expertise and communication skills. The ideal candidate will have a deep understanding of pharmacovigilance principles and practices, as well as excellent analytical and problem-solving skills.
Benefits: As a member of this team, you will contribute to the development of effective pharmacovigilance strategies that prioritize patient safety and product integrity.
Others: The successful candidate will be part of a dynamic team that prioritizes collaboration, innovation, and excellence in pharmacovigilance services.
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