The Clinical Trials Center of the VA Pittsburgh Healthcare System is recruiting for a clinical research coordinator to staff a multifaceted clinical research program.

The incumbent will coordinate and implement procedures according to study protocol including screening, administering informed consent, conducting protocol related visits consisting of but not limited to collection, processing and shipment of blood specimens as well as  collecting data from patient medical records, interviews, questionnaires, diagnostic tests and other sources. Ensure compliance with protocol guidelines and requirements of regulatory agencies; identify problems and/or inconsistencies and monitor patients' progress to include documentation and reporting of adverse events; recommend corrective action as appropriate. The incumbent will also assist with regulatory preparation as well as attending investigator meetings as required. Experience in the conduct of phase II-IV drug/device trials is recommended. ACRP or SOCRA certification required. Salary will be commensurate with experience