Senior Clinical Research Coordinator (Sr. CRC) – Los Angeles, CA (90033)
Position Overview:
This role is with a fast-paced clinical site experiencing significant demand and expansion. We are seeking a Senior Clinical Research Coordinator (Sr. CRC) 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:
- 3+ 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.
