PRMS Program Coordinator – Clinical Research Trials

Role Overview

• 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