Clinical Research Coordinator
University of Pittsburgh
Job Summary
Conducts research assessments on study participants. Assists with and adheres to Institutional Review Board (IRB) renewal, modification, and approved protocols. Assists with training staff. Ensures adherence to protocols and corrects issues with data collection.
a. Must be able to use a PC or laptop, and familiar with Microsoft Office, including Excel. Similarly, must be able to use both a tablet and smartphone as part of research protocols.
b. Must be able to communicate effectively with patients, providers and other members of the research tea.
c. Must be able to adhere to research protocols and follow Good Clinical Practice standards.
d. Must be able to perform phlebotomy, or willing to learn to perform phlebotomy.
a. must be able to sit or stand for prolonged periods of time.
b. must be able to walk 1-2 blocks for sample delivery, if necessary
c. must be able to lift up to 20 pounds at times.