Clinical Research Coordinator - 248849

Clinical Research Coordinator – Los Angeles, CA (90033)

Position Overview:

This role is with a fast-paced clinical site experiencing significant demand and expansion. We are seeking a Clinical Research Coordinator to support our growing team and lead the execution of clinical trials. This new site-based role requires someone who thrives in high-paced settings and is dedicated to high-quality patient care and research integrity. Our ideal candidate will manage a significant portion of the studies, ensuring all aspects of trial conduct are executed efficiently and in compliance with regulatory guidelines.

Key Details: Location:

Los Angeles, CA (90033) Pay:

$35-$40/hour Schedule:

Monday – Friday, standard business hours.

Primary Duties and Responsibilities: See an average of 5 patients per day for clinical trial visits, including follow-up and new patient assessments for a wound care trial. Conduct and document patient visits, including source documentation and entry of data into Electronic Data Capture (EDC) systems. Perform weekly patient progress monitoring using ECare, including wound care assessments and photo documentation to track and assess changes over time. Assist with continuing Institutional Review Board (IRB) submissions as needed; initial IRB submissions will typically involve central IRBs and are not the primary responsibility. Carry out study close-out activities in accordance with protocol, site, and regulatory standards. Coordinate patient visit schedules, allocating appropriate time blocks based on the complexity of visits (e.g., 2 hours for new visits and 1 hour for follow-ups). Collaborate directly with senior research staff, including the clinical research lead to maintain and improve the quality of clinical research operations.

Candidate Requirements: 2+ years as a Clinical Research Coordinator (CRC) Experience in wound care and diabetes (preferred) Fluent in English and Spanish Phlebotomy certificate or Medical Assistant Experience in patient-facing roles Experience in IRB submissions, source documentation, and trial management A thorough understanding of regulatory requirements and principles of GCP

Team Environment and Support: You will work closely with a dedicated team of coordinators and have access to robust support systems within the clinical network. We value a culture of collaboration, adaptability, and excellence in clinical care and research.