CLINICAL RESEARCH COORD A

Duties: Prepare protocols, informed consents, and advertisements for regulatory approval. 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. Interface with regulatory authorities; 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.

Qualifications: BS degree and 1 to 3 years research experience or an equivalent combination of education and experience required. Must be able to work flexible hours.

Reference Number: 40-26746

Salary Grade: 025

Employment Type: Exempt

Org: WM-Ctr for Res on Reprod and Women's Health

Special Requirements: Background check required after a conditional job offer is made. Consideration of the background check will be tailored to the requirements of the job.

Job Family: I-Technical/Professional Research