Clinical Research Coordinator, Regulatory Compliance
Overview
As a Clinical Research Coordinator, you will own the execution of clinical protocols at our Inglewood site, supporting 5+ active studies with a focus on participant safety and data integrity. You'll work directly with the Principal Investigator and senior research staff, collaborating with cross-functional teams including data management and regulatory affairs. This contract role stands out for its hands-on involvement in the full study lifecycle, from screening to closeout, in a fast-paced research environment.
What You'll Do7
- 1Screen participants for eligibility by collecting medical history and vital signs, using EDC systems to document findings.
- 2Obtain informed consent from participants, ensuring compliance with ICH-GCP guidelines and institutional review board requirements.
- 3Schedule study visits and procedures, coordinating with clinical teams to meet protocol timelines.
- 4Maintain accurate source documentation and case report forms, entering data into CTMS platforms.
- 5Educate participants on study requirements and monitor adherence to protocols, addressing questions or concerns.
- 6Report adverse events and protocol deviations to the research team, documenting actions taken.
- 7Support study closeout activities, including data query resolution and file archival.
Requirements6
- 1High school diploma or equivalent; associate's degree or higher in a health-related field preferred.
- 22+ years of experience in clinical research coordination, with hands-on participant screening and informed consent.
- 3Proficiency with electronic data capture systems and clinical trial management software.
- 4Advanced skills in Microsoft Excel, Word, and PowerPoint.
- 5Current CPR/BLS certification required.
- 6Certification as a Clinical Research Coordinator (CCRC) or willingness to obtain within 1 year.
Salary Insight
$26 - $30k per year
Location
Required Skills
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