US Licensed Associate Director, Pharmacovigilance
Job Summary
Leading global pharmacovigilance projects, the full-time US Licensed Associate Director, Pharmacovigilance will provide strategic oversight and operational management of pharmacovigilance services in a remote setting, ensuring compliance with regulations and quality standards while guiding teams through complex safety reporting challenges.
Key responsibilities
- Lead global pharmacovigilance projects and teams, ensuring compliance with regulations and project timelines
- Provide strategic oversight of staff and project performance, addressing risks and issues to support study execution
- Guide teams on complex safety reporting scenarios, serving as a key point of expertise and decision-making
Required qualifications
- Bachelor's degree in a science-related field, nursing, or equivalent experience
- Minimum of 8 years of global pharmacovigilance experience in pre-approval clinical trials
- At least 2 years of demonstrated leadership experience in a people, project, or departmental capacity
- Strong knowledge of global pharmacovigilance regulations and clinical trial best practices
- Proven experience managing budgets, timelines, and cross-functional stakeholder relationships
Complete Job Description
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