Responsible for implementation of pharmacoepidemiology strategy
Generation of real world evidence (RWE)
Conduct of regulatory-agency required epidemiologic studies for post-marketing commitments (e.g., PASS, PAES, PMR, DUS, effectiveness of REMS and RMMs)
Actively contribute to other pharmacoepidemiologic activities as a subject matter expert
Collaborate with Global Patient Safety Leads, Safety Scientists, Regulatory Affairs, Clinical Scientists and other interested parties
Provide timely epidemiological and risk management support to project and product teams
Actively participate in process improvement activities within the department and Global Patient Safety (GPS) as needed
Requirements
MD, PharmD, plus other post-graduate degree in epidemiology or a related field (e.g. MPH, MSc)
Doctoral degree in epidemiology or a related field, generally with <3 years of relevant post-doctoral experience
Other post-graduate degree in epidemiology or a related field (e.g. MPH, MSc), generally with 2+ years of relevant experience.
Industry/Regulatory experience preferred.
Benefits
annual bonuses or other incentive plans
equity awards
pension or retirement benefits
401(k) company match
health and wellness programs
fitness centers
insurance benefits (e.g. medical, dental, vision, life and disability)