Clinical Research

• Provide expert guidance during reconciliation of unit patient charges to ensure appropriate billing
• Identify and implement changes in clinical trial protocol calendar setup
• Provide training and resources related to research billing to study teams
• Oversee research billing compliance activities
• Advise researchers on proper setup and execution of billing activities for clinical-trial patients
• Interpret complex clinical trial protocols using research billing rules, clinical workflows, sponsor requirements, and electronic system capabilities
• Configure and review study calendars and budget setup for clinical trials
• Perform Medicare coverage analysis for complex research studies
• Work with study teams to ensure billing compliance
• Develop and implement internal quality-control processes for accurate calendar and budget builds

Clinical Research Billing Compliance Specialist

• Plan staff implementation of protocols and ongoing quality review for basic or moderately complex clinical research trials or programs
• Develop and monitor program budgets and review and approve expenditures
• Supervise at least 2.0 full-time equivalent employees, including hiring, performance management, discipline, and approval of hours worked
• Compose, assemble, and submit grant proposals and protocols according to applicable rules and regulations
• Compile audits and document research data to ensure compliance with institutional policies and procedures
• Analyze research portfolios and accounts, solicit internal and external research opportunities, promote unit capabilities, and recommend strategic program enhancements to leadership
• Provide strategic and operational oversight for clinical research programs
• Oversee clinical trial operations and regulatory compliance
• Collaborate with investigators, sponsors, regulatory bodies, and institutional partners

Clinical Research Manager

• Perform day-to-day administrative activities of the clinical research trials program
• Provide support to facilitate achievement of the program’s goals
• Recruit, screen, enroll, and obtain consent from program participants
• Conduct or coordinate training for program participants
• Coordinate research protocols, appointments, procedures, and participant contact
• Collaborate with departments and institutions
• Collect, analyze, and disseminate program data
• Report program data and progress to stakeholders
• Identify protocol implementation problems and communicate them to study investigators
• Assure compliance with IRB and regulatory agency requirements
• Assist with preparation of IRB documents and reports
• Assist in evaluation and writing of research protocols
• Collaborate on educational, marketing, website, form, and report materials
• Develop, implement, and maintain comprehensive program databases and files with the Principal Investigator
• Maintain program timelines and track deadlines
• Coordinate outreach activities and liaise with community organizations
• Perform other duties as assigned

Clinical Research jobs in Wisconsin

Clinical Research Billing Compliance Specialist

Clinical Research Manager

Clinical Research Coordinator