About the role
Responsibilities Clinical Research Assistant (CRA) provides support to the research team by collecting, entering, abstracting, and managing the study data for sponsor data systems, publication, or other reporting. The CRA may also assist the Clinical Research Nurse (CRN) and/or Clinical Research Coordinator (CRC) in the set-up and execution of clinical research protocol procedures and associated administrative responsibilities. In some cases, the CRA may coordinate retrospective, quality, and other non-therapeutic research trials under Principal Investigator direction. Additionally, the CRA is responsible to maintain research medical equipment; accurately maintain logs; perform protocol-related tasks as assigned (within scope of practice); inventory, store, order and maintain study-related equipment/ supplies.
Qualifications Required:
- One year in a research or healthcare setting
Desired
- One year in data entry or abstraction
- Associate Degree
- Certified Clinical Data Manager OR Certified Clinical Research Associate OR Certified Clinical Research Coordinator OR Certified Clinical Research Professional OR Certified Medical Assistant OR Certified Tumor Registrar
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