PRMS Program Coordinator – Clinical Research Trials
WVU Online
full-time
Posted on:
Location Type: Hybrid
Location: Morgantown • Virginia • West Virginia • United States
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About the role
- Provide high level strategic and operational oversight to WVUCI in fulfilling all CCSG Protocol Review and Monitoring System (PRMS) requirements
- Shape the long term vision for PRMS by identifying emerging regulatory trends
- Oversee the scientific review infrastructure for all clinical research protocols
- Direct the full operational lifecycle of protocol submission, review, approval, and ongoing monitoring
- Lead quality assurance initiatives by conducting systematic reviews of PRMS processes
- Build strong, collaborative relationships with investigators and other stakeholders
Requirements
- Bachelor’s Degree
- A minimum of two (2) years of experience in program management, administrative support, research coordination and/or project management in clinical research
- Any equivalent combination of related education and/or experience will be considered
- Excellent organizational skills
- Problem-solving skills
- Proficient typing skills
- Proficient with Microsoft Office Suite including Outlook, Word, and Excel
- Knowledge in writing and grammar
Benefits
- 37.5-hour work week
- 13 paid holidays
- 24 annual leave (vacation) days per year
- 18 sick days per year
- A range of health insurance and other benefits
- 401(a) retirement savings with 6% employee contribution match
- Wellness programs
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
program managementadministrative supportresearch coordinationproject managementquality assuranceprotocol submissionprotocol reviewprotocol approvalmonitoring
Soft Skills
organizational skillsproblem-solving skillscollaborative relationships
Certifications
Bachelor’s Degree