Full-Time Associate Director, Epidemiology

Associate Director (AD) of Epidemiology in Pharmacovigilance & Patient Safety leads the scientific strategy for pharmacoepidemiology and real-world evidence to support product development and safety across therapeutic areas.

Responsibilities:

1. Lead or contribute to the development of real-world evidence, including study design, protocol and statistical analysis plan development, and execution.
2. Conduct comprehensive literature reviews to support signal assessments, establish background rates, and develop risk management plans.
3. Deliver epidemiology content for core safety and regulatory documents.
4. Advance epidemiology research and methodologies, providing expertise on novel techniques.
5. Collaborate with global epidemiology teams and key partners.
6. Development of RWE studies to support asset and disease area strategies.

Qualifications:

PhD/PharmD with 3-5 years of experience, or MPH/MS with 5+ years in epidemiology.

Technical Expertise:

Demonstrated high level of methodology and technical expertise in regulatory real-world methods.

Communication Skills:

Ability to clearly communicate epidemiology concepts to diverse audiences.

Business Acumen:

Knowledgeable in current and future policies affecting the business.

Negotiation Skills:

Ability to negotiate in challenging situations.

Regulatory Knowledge:

Comprehensive understanding of adverse event collection, signal detection, and signal validation.

What is the last date for applying to the job?

Which countries are accepted for this remote job?