Clinical Research Coordinator I

2 weeks ago


Fresno, California, United States CEDARS-SINAI Full time
Job Summary

Cedars-Sinai is seeking a highly motivated and detail-oriented Clinical Research Coordinator I to join our Obstetrics & Gynecology Department. The successful candidate will be responsible for coordinating clinical research studies, ensuring compliance with regulatory requirements, and maintaining accurate records.

Key Responsibilities
  • Coordinate clinical research studies, including screening of potential patients, presenting non-medical trial concepts, and participating in informed consent processes.
  • Schedule patients for research visits and procedures, and collaborate with physicians and medical personnel to document patient information.
  • Maintain accurate source documents, data collection, documentation, entry, and reporting, including timely responses to sponsor queries.
  • Compile and report on each study, including information related to protocol activity, accrual data, workload, and other research information.
  • Ensure compliance with federal and local agencies, including the FDA and local IRB.
  • Participate in required training and education programs, and maintain research practices using Good Clinical Practice (GCP) guidelines.
  • Maintain patient confidentiality according to HIPAA regulations and applicable law.
Qualifications

Educational Requirements:

  • High School Diploma/GED required
  • Bachelor's Degree in Science, Sociology, or related field preferred

Licenses:

  • SOCRA or ACRP Certification preferred upon hire

Experience:

  • One (1) year of clinical research-related experience required


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