Clinical Research Coordinator

1 day ago


Los Angeles, California, United States CEDARS-SINAI Full time
Job Summary

Cedars-Sinai is seeking a Clinical Research Coordinator I to join our team. The successful candidate will provide study coordination, screening of potential patients for protocol eligibility, and participate in the informed consent process.

Key Responsibilities
  • Coordinate clinical research studies, including screening patients for protocol eligibility and presenting non-medical trial concepts and details.
  • Schedule patients for research visits and procedures, and document thoroughly on Case Report Forms (CRFs).
  • Maintain accurate source documents related to all research procedures, and ensure compliance with federal and local agencies.
  • Responsible for accurate and timely data collection, documentation, entry, and reporting, including timely response to sponsor queries.
  • Participate in monitoring and auditing activities, and notify direct supervisor about concerns regarding data quality and study conduct.
  • Work closely with regulatory coordinators or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters.
  • May perform other regulatory / Institutional Review Board duties, budgeting duties, and assisting with patient research billing and reconciliation.
Requirements
  • High School Diploma/GED
  • 6 months Clinical research related experience
About Us

Cedars-Sinai is a leader in providing high-quality healthcare encompassing primary care, specialized medicine and research. We are committed to delivering coordinated, compassionate healthcare to our patients and communities.



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