Role OverviewThis position provides day-to-day activities of clinical trials, including monitoring of research participants, enrollment, and screening. The role requires flexibility and a detail-oriented individual to work closely with senior research staff.
What You Will Do
Coordinates day-to-day activities for research protocols, ensures accurate data collection, documentation, organization, and the safety of research participants, and may supervise and provide guidance to other research staff.
Why It Might Be a Fit
The ideal candidate will have a Bachelor's degree in a related field, four years of related experience may substitute for the degree requirement, and two years of relevant experience. Oncology research study experience and Spanish speaking are preferred qualifications.
Requirements
- Bachelor's degree in a related field
- Four years of related experience may substitute for degree requirement
- Two years of relevant experience
]]>