CLINICAL RESEARCH COORD A
Duties: The primary role of Clinical Research Coordinator is the organization, coordination and implementation of research studies for the MFMU network. The essential functions of the position include but are not limited to:
Detailed screening of patients for eligibility across multiple studies
Consenting of patients into multiple studies
Coordinate scheduling of trial participants visits with study investigators and nurse practitioners as per protocol. Collaborate with clinical team as necessary to provide a positive encounter. Provide clinical services, including phlebotomy and obtain biospecimens as required by the protocol. Intercept and respond to trial participants phone calls. Perform telephone follow-up per study protocol.
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 nurse coordinator and investigators as well as the patient.
Position is contingent on continued funding.
Qualifications: A Bachelor's Degree and 1 to 3 years of experience or an equivalent combination of education and experience required. Must be able to work flexible hours. Position requires a highly motivated, articulate individual with excellent oral and written communication skills. The candidate should possess the ability to work independently and also as part of a team. Strong planning, organizational and prioritizing capabilities along with problem solving skills desired.
Reference Number: 40-28943
Salary Grade: 025
Employment Type: Exempt
Org: WM-Ctr for Res on Reprod and Women's Health
Job Family: I-Technical/Professional Research