Clinical Research Coordinator

1 week ago


San Diego, California, United States CEDARS-SINAI Full time
Clinical Research Coordinator I - Medicine/Endocrinology

Cedars-Sinai is seeking a highly motivated and detail-oriented Clinical Research Coordinator I to join our team in the Department of Medicine, Endocrinology Division. As a key member of our research team, you will play a critical role in supporting the coordination of clinical trials and studies, ensuring the highest level of quality and compliance with regulatory requirements.

Key Responsibilities:
  • Schedule and coordinate research visits and procedures for patients participating in clinical trials.
  • Collaborate with physicians and medical personnel to document patient information, adverse events, and protocol compliance on Case Report Forms (CRFs).
  • Maintain accurate and up-to-date source documents related to research procedures.
  • Participate in monitoring and auditing activities to ensure compliance with Good Clinical Practice (GCP) guidelines.
  • Notify supervisors of concerns regarding data quality and study conduct.
  • Work closely with regulatory coordinators and the Institutional Review Board (IRB) to submit adverse events, protocol deviations, and safety letters.
  • Perform other regulatory and Institutional Review Board duties, budgeting duties, and assist with patient research billing and reconciliation.
Requirements:
  • High School Diploma/GED, required.
  • Bachelor's degree in a Science, Sociology, or related field is preferred.
  • One (1) year of clinical research experience, required.
  • ACRP/SoCRA certification is preferred.

Cedars-Sinai is a leader in providing high-quality healthcare, and we are committed to creating a work environment that is inclusive, diverse, and supportive of our employees' growth and development. If you are a motivated and detail-oriented individual who is passionate about clinical research, we encourage you to apply for this exciting opportunity.



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