Medical Director, Neuroscience, Global Patient Safety
$160,500–$305,000 year
HybridNorth Chicago, Illinois, United States
Job Summary
Conduct safety surveillance and characterize product safety profiles for pharmaceutical, biological, and drug-device combination products throughout their lifecycle. Lead and oversee key pharmacovigilance activities, including signal detection, risk management strategy implementation, and the development of medical safety assessments, regulatory responses, and periodic safety reports. Analyze aggregate safety data and clinical information to communicate findings to cross-functional teams and regulatory authorities. Effectively write, review, and present technical documents while independently evaluating and making decisions in complex environments. Mentor team members and guide analysis of clinical data and epidemiological information.
Required Qualifications
- MD / DO
- 2+ years of residency with patient management experience
- 2-5 years of Pharmacovigilance / Clinical Development experience in the pharmaceutical industry
- Fluency, both written and oral, in English
- Ability to lead cross-functional teams in a collaborative environment
- Ability to evaluate and make independent decisions
- Ability to work effectively in the situation of uncertainty and complexity
- Ability to multitask
Desired Qualifications
- Master Public Health
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