Associate Medical Safety director
IQVIA(1 month ago)
About this role
This role provides medical expertise to evaluate safety data from clinical trials and post-marketing sources as part of the pharmacovigilance process. The position serves as a senior technical leader supporting product safety surveillance and scientific assessment of serious adverse events within a product’s safety profile and therapeutic area. It collaborates closely with post-marketing safety experts and safety surveillance groups and supports oversight activities for selected products.
Required Skills
- Pharmacovigilance
- Medical Review
- Adverse Events
- Case Assessment
- Causality Assessment
- Expectedness Review
- MedDRA Coding
- Safety Narratives
- Aggregate Reports
- DSUR
+11 more
Qualifications
- MD
- Medical License
About IQVIA
iqvia.comIQVIA is a leading global provider of data, technology, and advanced analytics focused on transforming healthcare and life sciences. The company empowers organizations to accelerate innovation, enhance patient outcomes, and expedite the market introduction of new treatments through comprehensive healthcare analytics and real-world evidence. With a commitment to Human Data Science, IQVIA combines its extensive expertise with innovative technology to improve health outcomes worldwide.
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