Hepatology - Medical Monitor
Core
Provide medical, scientific, and strategic leadership for the planning, execution, and reporting of clinical trials in Hepatology.
Role type
Medical Monitor (Clinical Trials)
Builds
Clinical Study Reports, regulatory documents, manuscripts, and new clinical project designs
Domain
Clinical Research / Hepatology
Deliverable
client delivery
Required skills
Medical management, study design, protocol development, safety issue management, regulatory document contribution, manuscript writing, cross-functional coordination
Preferred skills
Board certification, current medical licensure, prior clinical trial research experience, pharmaceutical-related clinical research experience
Technologies
Clinical trial management systems, regulatory document platforms
Responsibilities
Provide medical management and expertise for clinical trials; Contribute medical expertise to study reports, regulatory documents, and manuscripts; Manage safety issues in clinical trials; Participate in new business development through proposal and sponsor meetings; Coordinate with other departments in all phases of studies; Follow specific research protocols and lead adherence to policies
Seniority
Mid-Senior, hands-on IC