PART TIME CLINICAL RESEARCH COORDINATOR

Duties: The clinical research coordinator will support the Pulmonary Vascular Disease Program investigators and research staff. Screen, recruit, consent and enroll eligible subjects using GCP guidelines. Provide education to the patient and/or families. Responsible for management of a comprehensive clinical database for pulmonary hypertension, accurate data collection and data entry of clinical data on study subjects; coordination, organization and management of documentation related to the database. Responsible for drawing labs (phlebotomy training preferred), sample processing and shipping. Responsible for the preparation and processing of all Institutional Review Board (IRB) documentation through the IRB and defined regulatory authorities, including submissions, continuing reviews, amendments and adverse event reporting. Communicate any research issues to PI and primary MD, communication with research team, including Investigators, project managers, CRC and regulatory team, to ensure patient safety and proper study conduct. Demonstrate vigilance in patient safety, protocol compliance, and data quality. Other duties as assigned. Perform these tasks with minimal supervision after initial training.

Qualifications: A Bachelor's degree and 1 to 3 years of experience or equivalent combination of education and experience required. Pulmonary expertise preferred. Phlebotomy experience preferred. Effective communication and writing skills; ability to multi-task and problem solve; Energetic, interactive and demonstrated ability to work as part of a team as well as independently; knowledge of IRB and human research protection regulations. Must possess strong computer skills and be able to independently and proficiently work in MS office suite. Position contingent upon funding.

Reference Number: 40-26485

Salary Grade: PT/25

Employment Type: Non-Exempt

Org: DM-Pulmonary, Allergy and Critical Care

Special Requirements:

Job Family: Z-Non-Classified Staff/Non-Unionized Job Grades