Clinical Research

• Provide a high standard of care for participants in clinical trials and respond to emergency situations according to clinical research standards
• Perform routine monitoring and close-out of clinical sites
• Maintain study files
• Conduct pre-study and initiation visits
• Liaise with vendors
• Manage study sites according to project plans
• Ensure study staff receive proper materials and instructions
• Verify informed consent procedures and protocol requirements comply with applicable regulations
• Verify data integrity in Case Report Forms and other data collection tools
• Monitor data for missing or implausible information
• Manage registries and undertake feasibility work when requested
• Complete Serious Adverse Event reporting, reports, narratives, and follow-up
• Perform CRF review, query generation, and resolution using Fortrea or client data management systems
• Assist with training new employees through activities such as co-monitoring
• Coordinate designated clinical projects as a Local Project Coordinator
• Act as a local client contact when assigned
• Travel frequently to client and site locations, including occasional domestic and international travel
• Perform other duties assigned by management

Clinical Research Associate 2 – Oncology

• Provide research project support to requesting departments
• Coordinate routine to moderately complex research projects and manage related communication and documentation
• Support clinical research studies and departments across the Intermountain system
• Coordinate IRB/HRPP submissions and support research oversight committees and programs, or coordinate administrative and technical functions for grants, contracts, and external funding agreements
• Define, develop, and execute clinical research project plans, work plans, and schedules
• Identify resources, roles, and responsibilities for assigned studies
• Facilitate feedback from key participants and participate as a team member
• Develop budgets and scope documents for clinical research studies
• Assist with business cases, proposals, budgets, and required internal and external routing forms
• Analyze study requirements and communicate impacts to stakeholders
• Participate in quality assurance plans and reviews
• Document deliverables, track and communicate timelines, and prepare reports and presentations
• Support research billing by reviewing research accounts and reconciling invoices
• Manage study startup, maintenance, and closeout activities
• Support study teams on study financials and act as a subject-matter expert and liaison
• Provide backup support as a clinical research coordinator when requested
• Develop Medicare Coverage Analysis documents, review reimbursement guidelines, ensure correct billing, and provide coverage review
• Coordinate project assessments and response planning
• Communicate risks, develop and execute mitigation strategies, and lead auditing activities for compliance

Clinical Research jobs in Utah

Clinical Research Associate 2 – Oncology

Clinical Research Project Coordinator