The project manager will work closely with the Principal Investigators, senior project manager, and independently to plan and implement all phases of a large (9,000 subjects) multi-site POCRI funded clinical trial conducted in the United States. Responsibilities include assisting in site start-up; IRB preparation of protocols, amendments and continuing reviews as well as maintaining compliance with IRB requirements using both local and central IRBs. In addition, the candidate will work closely the training and supervision of the research assistants who are the primary contacts for the sites and ensures proper handling of site issues and questions. The candidate must have the ability to work independently, as well as working with other research staff, both professional and non-professional, excellent written and oral communication skills, attention to detail, and ability to prioritize a variety of tasks. The project manager will be responsible for the development, refinement, and implementation of study procedures and preparation of data.
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