CLINICAL RESEARCH COORD A
Duties: Coordinate scheduling of trial participants' visits with study investigators and nurse practitioners as per protocol. Provide clinical services, including phlebotomy, and obtain biospecimens as required by the protocol. Plan, direct, and assess overall study management of patient in collaboration with investigator. Intercept and respond to trial participants' phone calls. Perform telephone follow-up per study protocol.
The coordinator is also responsible for data collection and management in accordance with study protocol and the maintenance of source documents and case report forms. Collect and report timely, valid, accurate data, maintain individual patient records. Maintain study compliance and integrity through close collaboration with investigator as well as the patient.
Provide ongoing service education updates to all investigators and HUP staff who have eligible participants for clinical research studies.
Position is contingent on continued funding.
Qualifications: BS degree and 1 to 3 years of research experience, or equivalent combination of education and experience, are required. Must be able to work flexible hours.
Reference Number: 40-27464
Salary Grade: 025
Employment Type: Exempt
Org: WM-Ctr for Res on Reprod and Women's Health
Job Family: I-Technical/Professional Research