Senior Clinical Research Coordinator

Duties

• P Practices and adheres to the “Code of Conduct” philosophy and “Mission and Value Statement”
• Assist with training CRC Level I and II personnel
• Act as a role model to peers
• Perform routine operational activities for multiple research protocols
• Liaise between site research personnel, industry sponsors, and Supervisor
• Collaborate closely with various site departments/teams, including finance, relevant hospital administrative representatives, and the local IRB, if applicable
• Cookordinate schedule of assessments from initial submission of feasibility until study closeout
• Cookordinate submission and approval for the Site’s Facility Review Committee, if applicable
• Provide awareness of research protocols to appropriate site-level personnel, including physicians, nurses, clinical staff, and administrators
• Document all specific tasks required by the protocol (i.e. medication forms, quality of life questionnaires, neuro exams, vital signs sheets, times of lab draws, etc.)
• Accurately perform/calculate and documents the BSA, mRS, NIHSS, STS risk score, or any other approved CRC task, as needed per protocol
• Document all patient, staff, and sponsor correspondence, including follow-up encounters, adverse events, interventions, pharmacy dispensations, and patient phone calls
• Accurately complete all data requests (including queries) and submit with source documentation within the timeframe specified in the SOP
• Re-consent patients in a timely manner and document process appropriately
• Support study team in mitigating risks and optimizing site compliance
• Work with site personnel and local investigators to assess site feasibility and performance
• Regularly meet with physicians and administrators, when applicable, to assess study performance and investigator satisfaction
• Collaborate with other departments (non-invasive, finance, laboratory, etc.) to develop and implement processes in support of the research activities
• Assist with providing a research update during Site Administrative meetings (Section meetings, Site Service Line meetings, etc.)

Qualifications

• Education: Bachelor’s degree required Master’s degree preferred
• Experience: 1+ years of relevant experience required 5+ years of relevant experience preferred
• Licenses, Certifications, & Training: Certified Clinical Research Coordinator (ACRP or CCRP) preferred