Head of Multiple Myeloma & AML, Oncology - Global Patient Safety

📋 Description

• Understanding and application of the pharmacology, chemistry and non-clinical toxicology to
• Responsible for safety surveillance for pharmaceutical / biological / drug–device combined products
• Lead and set the strategy for key pharmacovigilance documents, including but not limited to
• Apply current regulatory guidance as appropriate for safety surveillance and authorship of PV
• Analyze and interpret aggregate safety data and communicate these analysis and interpretation to
• Effectively write, review and provide input on technical documents independently

🎯 Requirements

• MD / DO with 2+ years of residency with patient management experience
• Master Public Health is preferred in addition to MD / DO, not required
• 8 - 10 years of Pharmacovigilance / Clinical Development experience in the pharmaceutical industry
• Effectively analyze and guide analysis of clinical data and epidemiological information
• Effectively present recommendations / opinions in group environment both internally and externally
• Write, review and provide input on technical documents