Research Protocol Analyst
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Job Description
Research Protocol Analyst managing compliance and documentation for clinical trials. Overseeing human research protocols at City of Hope to ensure regulatory adherence and ethical standards.
Responsibilities:
- Manage the full lifecycle of research protocol review—pre‑reviewing submissions, coordinating expert committee evaluations, preparing regulatory documentation, and ensuring timely, compliant investigator responses
- Prepare complete meeting materials, provide regulatory guidance for complex submissions
- Support external IRB oversight by quality‑checking informed consent language
- Assist with preparation for internal and external audits
- Contribute to quality‑improvement efforts by identifying process efficiencies
Requirements:
- Bachelor’s degree (3 additional years of experience plus the minimum experience requirement may substitute for minimum education)
- At least 2 years of experience in the academic/clinical research review setting
- Preferred qualifications: Certified IRB Professional (CIP), Certified Clinical Research Professional (CCRP), or Certified Clinical Research Coordinator (CCRC)
- Experience in review and processing of research protocols in an academic research setting.
Benefits:
- Comprehensive Benefits
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