Medical Monitor
Core
Provide medical, scientific, and strategic leadership for the planning, execution, and reporting of clinical trials across multiple therapeutic areas.
Role type
Medical Monitor (Clinical Research)
Builds
Clinical Study Reports, regulatory documents, manuscripts, and new clinical project designs
Domain
Clinical Research / Contract Research Organization (CRO)
Deliverable
client delivery
Required skills
Medical management, study design, protocol development, safety issue management, regulatory document contribution, manuscript preparation, cross-functional coordination
Preferred skills
Board certification, current medical licensure, pharmaceutical-related clinical research experience
Technologies
Clinical trial management systems, regulatory document platforms
Responsibilities
Provide medical expertise for clinical trials; manage safety issues in trials; contribute to study reports and manuscripts; participate in new business development and proposal meetings; coordinate with departments on feasibility and design; lead adherence to research protocols
Seniority
Mid-level to Senior, hands-on IC