GLOBAL MEDICAL SAFETY EXPERT BIOSIMILARS
On-site · Bogotá, Bogota D.C., Colombia
Job Summary
Lead pharmacovigilance activities for biosimilars, serving as a single point of contact for Biosimilars in LATAM and worldwide. Represent Abbott before governmental/regulatory authorities on pharmacovigilance topics. Develop strategic risk management plans for assigned products; review protocols, reports, and publications; provide safety expertise across all stages of global drug development; ensure safety monitoring strategy and reference safety documents throughout a product lifecycle; collaborate with QPPV, safety representatives, and cross-functional teams; work largely independently with some oversight; located in Bogotá, Colombia.
Required Qualifications
- Doctor of Medicine (MD)
- Minimum 5-8 years industry experience in Pharmacovigilance
- Fluent in English
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