Description:

Under general supervision of the Research Director, coordinates and manages all aspects of clinical studies involved in prostate and bladder oncology, including but not limited to subject screening, recruitment, data entering, abstracting, and assessment. Execute, manage, and coordinate research protocols, as directed by the Director of Research and/or Principal Investigator (PI); may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols and regulating agency policies.Support the management and coordinating the tasks of single or multiple clinical research studies, depending on their size and complexity; acting as an intermediary between services and departments while overseeing data and specimen collection; manage and report on study results, create, clean, update, and manage databases and comprehensive datasets as well as renewals and modifications of protocol applications and the implementation of new studiesDocument and maintain required records necessary for study activities per local, state, and FDA GCP requirements

Additional Skills & Qualifications:

Experience handling adverse eventsInterpreting/Gathering medical historyPhlebotomy experience neededPerforming vitals

Experience Level:

Expert Level

About Actalent

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