Plan, implement, evaluate, and complete full execution of assigned clinical trials; often functions as a global trial lead
Set goals, and timelines, provide oversight and positive leadership to foster motivation within the team
Provide oversight and coordination of the operational aspects of the functional areas on assigned projects to ensure compliance
Provide management of a full scope clinical trial projects including global trials from start-up through analysis phase
Provide coordination of a clinical trial project including organization, implementation, and management of scoped activities
Evaluate and manage project budget against project milestones and scope
Regularly assess project profit margins and work with the trial-assigned Director and project team to understand deficiencies
Prepare or provide oversight and guidance in the development of trial required deliverables
Serve as client contact at project operational level
Provide oversight to contracted vendors and review specifications

Bachelor’s degree in allied health fields such as nursing, pharmacy, health or natural sciences
At least 6 years of clinical research experience (CRO CRA or Research Manager, Site Research Manager, Central Clinical Research Laboratory Manager)
Graduate degree preferred
Previous technical and managerial experience in conducting clinical pharmaceutical research studies in a hospital setting, a pharmaceutical company, or CRO
Previous CRA experience preferred
Experience or education indicating knowledge of medical and pharmaceutical terminology preferred
Previous experience in a Clinical Project Manager or Clinical Trial Manager level position preferred

Clinical Project Manager III – Senior

Key skills