Duties include but are not limited to:· Practices and adheres to the "Code of Conduct" philosophy and "Mission and Value Statement" · Demonstrate ability to fulfill responsibilities and duties of the CRC Level I and II · Assist with training CRC Level I and II personnel · Act as a role model to peers Clinical Research Operations: · 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 · Coordinate schedule of assessments from initial submission of feasibility until study closeout · Coordinate 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 · Ensure follow-up appointments, imaging, or any related procedures are scheduled correctly according to protocol requirements · 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 Site Development: · 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.) · Able to guide research team members on the management of non-compliant data and/or study activities Reporting and Analysis: · Monitor patient enrollment at the site through weekly reports, and reports results to Supervisor · Facilitate continuing education and training to investigators, as applicable Education: · Bachelor's degree required · Master's degree preferred · 1+ years of relevant experience required · 5+ years of relevant experience preferred Licenses, Certifications, & Training: · Certified Clinical Research Coordinator (ACRP or CCRP) preferred Benefits HCA Florida Mercy Hospital, offers a total rewards package that supports the health, life, career and retirement of our colleagues. Address: HCA Florida Mercy Hospital: 3663 S Miami Ave, Miami, FL 33133 Job Summary and Qualifications Senior Clinical Research Coordinator is responsible for coordinating multiple research protocols; serving as a liaison with local investigators and research personnel; and acting as a central resource for assigned research projects.