Accountable for the medical & scientific integrity of the study and the wellbeing of patients enrolled in clinical trials
Job Summary
Accountable for the medical & scientific integrity of the study and the wellbeing of patients enrolled in clinical trials.
Responsible for timely delivery of a quality protocol, clinical execution of complex clinical trials, and supports interpretation of clinical trial data.
Eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 25.0% of the base salary and eligibility for long term incentive program, plus comprehensive benefits.
Matching Summary
Accountable for the medical & scientific integrity of the study and the wellbeing of patients enrolled in clinical trials.
Salary
Base: $239,900.00 - $399,800.00; Bonus/Equity: 25.0% bonus target and share-based long term incentive; Benefits: Comprehensive and generous benefits package
Skills & Requirements
Must-have
medical monitoring of clinical trials
protocol design and development
safety data review
investigator and site engagement
regulatory compliance and reporting
Nice-to-have
cardiometabolic disease experience
leadership and team development
influencing and collaboration skills
Key Requirements
MD or equivalent medical degree
4+ years Clinical Development experience
2+ years licensed to prescribe medicines
Clinical research experience in phase 3/pivotal space