Research Protocol Analyst
Foundation
full-time
Posted on:
Location Type: Remote
Location: United States
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Salary
💰 $37 - $57 per hour
About the role
- 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
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
research protocol reviewregulatory documentationquality-checkingprocess efficiencies
Soft Skills
coordinationcommunicationattention to detail
Certifications
Certified IRB Professional (CIP)Certified Clinical Research Professional (CCRP)Certified Clinical Research Coordinator (CCRC)