Co-chairs clinical study teams and provides point of accountability for the design, conduct, interpretation, and reporting of clinical studies
Job Summary
Co-chairs clinical study teams and provides point of accountability for the design, conduct, interpretation, and reporting of clinical studies.
Designs and writes clinical trial outlines, protocols, and amendments, collaborating with internal and external experts to ensure efficient and objective-driven protocols.
Serves as a clinical site liaison, supporting trial conduct, building relationships with site staff, and ensuring understanding of protocol requirements.
Matching Summary
Co-chairs clinical study teams and provides point of accountability for the design, conduct, interpretation, and reporting of clinical studies.
Skills & Requirements
Must-have
Clinical study design and conduct
Protocol development and amendments
Good Clinical Practices (GCP)
Safety data review and escalation
Regulatory compliance for clinical trials
Nice-to-have
Collaborative study team leadership
Investigator engagement and site liaison
Data Monitoring Committee oversight
Publication and presentation support
Key Requirements
M.D., Ph.D., D.V.M., M.S., and/or PharmD or equivalent qualifications
Thorough understanding of local and international regulations
Practical experience in clinical trial strategies, methods, and processes
Track record of design, oversight, and interpretation of clinical studies
Knowledge and experience in Good Clinical Practices (GCP)