Clinical Trials Specialist

2 weeks ago


Modesto, California, United States Cedars-Sinai Full time
Job Summary

The Clinical Research Coordinator I role at Cedars-Sinai involves coordinating clinical trials and ensuring compliance with regulatory requirements. This part-time, hybrid position requires one year of experience in clinical research and certifications such as SOCRA or ACRP.

We offer a competitive hourly rate of $34.50-$41.65, plus benefits and opportunities for career advancement.

Key Responsibilities
  1. Screen patients for protocol eligibility and present trial concepts to participants.
  2. Document patient data accurately and timely, adhering to Good Clinical Practice guidelines.
  3. Maintain patient confidentiality according to HIPAA regulations and applicable law.
  4. Collaborate with the Institutional Review Board (IRB) and submit Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters as needed.
Qualifications
  • Bachelor's Degree in Science, Sociology, or related field (desired).
  • One year of clinical research experience (required).
  • SOCRA or ACRP certification (optional).


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