Base: $109,148.80 to $143,257.80; bonus/equity: an...
Hybrid
Post-authorisation safety studies
Targeted and systematic literature reviews
Rapid data analytics on large electronic healthcare data
The Safety Epidemiology team is responsible for the planning and execution of post-authorisation safety studies intended for submission to various health authorities
Job Summary
The Safety Epidemiology team is responsible for the planning and execution of post-authorisation safety studies intended for submission to various health authorities.
Responsibilities include designing, executing, analyzing, and reporting studies under the highest scientific standards and performing targeted and systematic literature reviews.
The team also sets the epidemiological strategy for FDA clinical trial diversity plans and conducts diversity-focused pharmacoepidemiology studies.
Matching Summary
The Safety Epidemiology team is responsible for the planning and execution of post-authorisation safety studies intended for submission to various health authorities.
Salary
Base: $109,148.80 to $143,257.80; Bonus/Equity: Annual Variable Pay Bonus/Short Term Incentive opportunity and equity-based long-term incentive program; Benefits: Competitive Flex Benefits & Retirement Savings Program, 4 weeks’ paid vacation, and annual Personal Days
Skills & Requirements
Must-have
post-authorisation safety studies
targeted and systematic literature reviews
rapid data analytics on large electronic healthcare data
epidemiological strategy for FDA clinical trial diversity plans
advanced epidemiological theory and techniques
critical appraisal to study designs
Nice-to-have
collaborative culture
knowledge-sharing and ambitious thinking
individualized flexibility
dedication to sustainability
dynamic, inclusive and supportive environment
Key Requirements
Ph.D. in pharmacoepidemiology, epidemiology or related health science field
Substantial hands-on experience in a research environment
Able to work effectively with internal & external collaborators
PhD dissertation in pharmacoepidemiology or epidemiology with a strong focus on medicines
Drug safety experience in a clinical or post-marketing environment
Knowledge and experience with drug safety reporting and regulatory compliance