Co-chairs clinical study teams and serves as the point of accountability for the design, conduct, interpretation, and reporting of clinical studies
Job Summary
Co-chairs clinical study teams and serves as the point of accountability for the design, conduct, interpretation, and reporting of clinical studies.
Provides clinical and scientific expertise to strategy and protocol development, ensuring efficient protocols through Enhanced Clinical Trial Design (ECTD) / Enhanced Quantitative Drug Development (EQDD).
Manages relationships with investigative sites, ensuring protocol adherence, addressing questions, and supporting enrollment activities while maintaining the 'Face of Pfizer' at sites.
Matching Summary
Co-chairs clinical study teams and serves as the point of accountability for the design, conduct, interpretation, and reporting of clinical studies.
Skills & Requirements
Must-have
Clinical study team leadership
Protocol development and design
Clinical trial strategy
Good Clinical Practices (GCP)
Safety data review
Regulatory compliance
Nice-to-have
Investigator engagement
Cross-functional collaboration
Mentoring and coaching
Continuous improvement
Key Requirements
M.D., Ph.D., D.V.M., M.S., and/or PharmD or equivalent
Postgraduate training in a medical discipline or drug development
Demonstrated scientific productivity
Understanding of local and international regulations
Practical experience in clinical trial strategies
Track record of clinical study design and oversight
Leadership or management experience
Experience in conduct and execution of clinical trials