Clinical Research

• Support Phase I–IV clinical trials at the WVU Cancer Institute
• Ensure compliance with institutional, state, federal, and international regulations, guidance, and policies
• Assess feasibility of implementing new protocols
• Collaborate with investigators, research staff, pharmacy, clinical staff, and ancillary departments to implement and conduct trials
• Facilitate and participate in monitoring and auditing reviews by regulatory, industry, IRB, and quality assurance agencies
• Serve as liaison between the research team, clinical staff, and sponsors
• Provide education and monitor protocol adherence throughout study lifecycles
• Support community outreach and trial advocacy
• Develop recruitment strategies and evaluate their effectiveness
• Conduct and document informed consent processes
• Educate patients about trial participation and provide study updates
• Assess eligibility, monitor adherence, schedule protocol tests and procedures, and perform in-scope study assessments
• Assess and document adverse events; collaborate on dose modifications and treatment responses
• Maintain source documentation and data reporting
• Provide protocol training and ensure proper documentation practices
• Update the Clinical Trial Management System with protocol and patient information
• Review trial budgets and coverage analyses
• Distinguish routine care from research-related expenses and ensure participant reimbursement or stipends
• Pursue oncology and clinical research education
• Lead projects or coordinate team efforts and assist with onboarding and training research staff

Clinical Research Coordinator

• Support Phase I–IV clinical trials at the WVU Cancer Institute
• Ensure compliance with institutional, state, federal, and international regulations, guidance, and policies
• Assess feasibility of implementing new protocols
• Collaborate with investigators, research staff, pharmacy, clinical staff, and ancillary departments to implement and conduct trials
• Facilitate and participate in monitoring and auditing reviews by internal or external agencies
• Serve as liaison between the research team, clinical staff, and sponsors
• Educate staff and monitor protocol adherence throughout study lifecycles
• Support community outreach and trial advocacy
• Develop recruitment strategies and evaluate their effectiveness
• Manage initial and ongoing informed consent processes
• Educate patients about trial participation and provide study updates
• Assess eligibility and monitor patient adherence
• Schedule and ensure adherence to protocol tests and procedures
• Perform study assessments and procedures within scope of practice, including vital signs, ECGs, and questionnaires
• Assess and document adverse events with investigators
• Collaborate on dose modifications and treatment responses
• Advocate for ethical participant care while adhering to protocols
• Maintain source documentation and data reporting
• Provide protocol training to clinical staff and research team members
• Update the Clinical Trial Management System with protocol and patient information
• Review trial budgets and coverage analyses
• Distinguish routine care from research-related expenses
• Ensure reimbursement of research expenses and protocol/contract stipends
• Participate in oncology and clinical research educational opportunities
• Lead projects or coordinate team efforts as needed
• Assist with onboarding and training research staff

Clinical Research jobs in Virginia

Clinical Research Coordinator

Clinical Research Coordinator – WVU Cancer Institute Clinical Research Unit