Clinical Research Coordinator IV managing complex clinical trials and supervising research administration staff. Handling compliance, budgets, and participant engagement strategies in a healthcare setting.
About the role
- PRMS Program Coordinator at WVU Cancer Institute ensuring scientific review and oversight for clinical research protocols. Supporting program operations and collaborating with stakeholders.
Responsibilities
- 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
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
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