Clinical trial project manager for multi-center international studies in neurological and other disorders. Bachelor’s degree with major course work in appropriate health, social science, or biological science field is required (advance degree preferred); or equivalent combination of education and experience. Requires a minimum of 2 years’ experience coordinating industry sponsored clinical trials. Extensive working knowledge of Good Clinical Practices (GCP) in clinical trials. Responsibilities involve planning, implementation and coordination of studies, including protocol development, model consent forms, writing operations manuals, conducting orientation meetings, maintaining regulatory documentation, liaising daily with site investigators and coordinators, working with data management processes, and assisting in leading team meetings to monitor progress in meeting study timelines. Must be a flexible team player with excellent written and verbal communication skills. Occasional travel may be required.
The University of Rochester is an equal opportunity employer.