Serve as a Global Point of Contact for Biosimilars and represent Abbott in interactions with governmental agencies on Pharmacovigilance matters
Job Summary
Serve as a Global Point of Contact for Biosimilars and represent Abbott in interactions with governmental agencies on Pharmacovigilance matters.
Develop strategic risk management plans, review clinical study protocols, and provide safety expertise throughout global drug development and product lifecycle management.
Lead the safety monitoring strategy, perform medical assessments, and ensure accountability for the safety of assigned EPD products, especially Biosimilars.
Matching Summary
Serve as a Global Point of Contact for Biosimilars and represent Abbott in interactions with governmental agencies on Pharmacovigilance matters.
Skills & Requirements
Must-have
Global Medical Safety Expert
Biosimilars expertise
Pharmacovigilance activities
Risk management plans
Regulatory framework understanding
Nice-to-have
Career development opportunities
Great place to work recognition
Diversity and inclusion focus
Key Requirements
Doctor of Medicine (MD)
Master's degree in Epidemiology, Clinical Pharmacology, or related field
Profound knowledge in Oncology esp. Treatment with Biologics
Hands on Experience with Biosimilars
Experience in people management
Minimum 8 years industry experience in Pharmacovigilance
Fluency in English
Broad and proficient understanding of Pharmacovigilance operations and regulatory frameworks