Sr Clinical Research Coordinator

Company: Joul--
Location: Riverside
Posted on: March 13, 2025

Job Description:

Title: Sr. Clinical Research Coordinator

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Location: Riverside, CA 92501 (Onsite)
Type/Duration: Contract
Schedule: M-F, 8a-5p
Rate: $30-34/hour

Position Summary
The 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. The individual in this role offers a significant contribution to the development of processes, tools, and training necessary to maintain site compliance and patient safety.

Major Responsibilities:
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 & Experience:
--- 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


Ref: #568-Clinical

Keywords: Joul--, Riverside , Sr Clinical Research Coordinator, Healthcare , Riverside, California