Clinical Research Coordinator - 254544

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.