Associate Director providing epidemiological insights for health and treatment outcomes at Pfizer. Conducting literature reviews and overseeing safety studies and regulatory submissions.
Responsibilities
Conduct comprehensive literature reviews and provide critical epidemiological insights
Assess epidemiological data and literature to support disease contextualization and regulatory submissions
Oversee epidemiological work with external vendors for literature reviews and regulatory deliverables
Design and implement innovative database studies to quantify risks
Conduct post-approval safety studies and develop strategies to address safety signals
Engage with regulatory agencies on safety epidemiologic issues and participate in Risk Management Committee activities
Requirements
BA/BS with 6+ years of experience or MBA/MS with 5+ years of experience or PhD/JD with 1+ year of experience or MD/DVM with any years of experience
Proficiency in writing, particularly for epidemiological sections of scientific documents
Strong computational skills and experience in statistical computing environments
Ability to drive large-scale changes within complex matrix organizations
Expertise in designing and implementing innovative database studies
Experience in conducting comprehensive literature reviews
Benefits
401(k) plan with Pfizer Matching Contributions
Additional Pfizer Retirement Savings Contribution
Paid vacation
Holiday and personal days
Paid caregiver/parental and medical leave
Health benefits including medical, prescription drug, dental and vision coverage
Job title
Associate Director, Safety Surveillance Research Scientist
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