Research Services Principal Professional – Clinical Research Nurse (part-time, hourly)

University of Colorado Anschutz Medical Campus

Department: Emergency Medicine

Job Title: Research Services Principal Professional – Clinical Research Nurse (part-time, hourly)

Position #:00851447 – Requisition #: 40667

Job Summary:

The Department of Emergency Medicine is currently seeking applications for a Research Services Principal Professional, Clinical Research Nurse. This is a part-time, hourly, University Staff (non-classified) position, for the Injury Generated by Burn and Frostbite (IGNITE) lab and the Airway, Trauma, Lung Injury, and Sepsis (ATLAS) Research Program. 

This role will participate in study start-up and documentation for clinical trials, as well as collaborate with clinical and research teams working to improve care of critically ill burn and frostbite patients at the University of Colorado Hospital. The projects focus on patients in the Emergency Department and Burn Intensive Care Units with critically injured burn and frostbite patients. The ideal candidate will have experience as a registered nurse, experience with research (clinical), collaborate effectively on multidisciplinary teams, and be highly detail oriented. 

Clinical Trial Process Improvement and  – 90%

• Assist with developing, or develop, protocol-specific systems and documents including process flows, training manuals, Standard Operating Procedures (SOPs) and Case Report Forms (CRFs). Maintains subject level documentation and prepares documents, equipment and/or supplies

• Assist with identifying issues related to operational efficiency and shares results with leadership

• Collect information to determine feasibility, recruitment and retention strategies.

• Employ, evaluate and assist with the implementation of innovative solutions to maximize recruitment and retention.

• Serve as a resource and participate in study initiation and close out duties.

• Collect, code, and analyze data obtained from research in an accurate and timely manner

• Adhere to research regulatory standards.

• Coordinate and administer patient care in compliance with protocol requirements.

Key Responsibilities:

Clinical Trial Process Improvement and Recruitment Support – 90%

• Assist with developing, or develop, protocol-specific systems and documents including process flows, training manuals, Standard Operating Procedures (SOPs) and Case Report Forms (CRFs). Maintains subject level documentation and prepares documents, equipment and/or supplies

• Assist with identifying issues related to operational efficiency and shares results with leadership

• Collect information to determine feasibility, recruitment and retention strategies.

• Employ, evaluate and assist with the implementation of innovative s