Job Title: Travel – Research RN (Non-Therapeutic)
Specialty: RN – Clinical Research
Location: 501 East Hampden Ave, Denver, CO 80113
Contract Type: Travel
Duration: 6 months - 1 year
Schedule: Monday – Friday, 7:00 AM – 4:00 PM

POSITION SUMMARY

The Research Nurse coordinates multiple research protocols, serving as a liaison between investigators, clinical staff, research teams, and sponsors. This role supports the operational, clinical, and regulatory aspects of human subject research, ensuring compliance with study protocols and timelines.

REQUIREMENTS

• Experience: Minimum 2 years as an RN; clinical research experience preferred.
• Certifications: Active RN license, BLS (required).
• Skills: Strong knowledge of research protocols, regulatory compliance, patient assessment, data management, and interdisciplinary communication.

Experience:

• Registered Nurse: 2 years (Required)
• Clinical research: 2 years (Required

• Practice and adhere to the “Code of Conduct” philosophy and “Mission and Value Statement”
• During your employment with HRI you will be routinely assigned training requirements. You are expected to complete any training assignments by the due date.
• Complete study medication order forms accurately, when needed, and has physician or appropriate designee sign orders prior to medication administration
• Perform routine operational activities for multiple research protocols * Liaise between site research personnel, industry sponsors, and Supervisor
• Collaborate closely with various site departments/teams, including finance, relevant hospital administrative representatives, and the local IRB, if applicable
• Coordinate protocol schedule of assessments from initial submission of feasibility until study closeout
• Coordinate submission and approval for the Site’s Facility Review Committee, if applicable
• Provide instruction on research protocols to appropriate staff, including interpretation of test results, observations, and related study data to physicians, nurses, and clinical staff
• Assess the patient and document findings at each clinic visit while on protocol
• Document all specific tasks required by the protocol (i.e. medication forms, quality of life questionnaires, neuro exams, vital signs sheets, times of lab draws, etc.)
• Complete the study medication order form accurately and have the physician or nurse practitioner sign orders prior to treatment
• Ensure that all medications are approved by the appropriate designee prior to initiating treatment or when changing medication regimens
• Accurately calculate and document the BSA, creatinine, STS calculation, or any other conversions needed, per protocol
• Document any interaction regarding the patient that occurs while the patient is enrolled on a protocol, including follow-up and survival (this includes home health intervention, pharmacies, and patient phone calls)
• Ensure that follow-up appointments, imaging, or any related procedures are scheduled correctly according to protocol requirements
• Accurately complete all data requests (including queries) and submit with source documentation within the timeframe specified in the SOP
• Generate and track drug shipments, device shipments, and supplies as needed
• Ensure timely and accurate data completion
• Track and report adverse events, serious adverse events, protocol waivers, deviations, and violations * Communicate all protocol-related issues to appropriate study personnel or manager
• Re-consent patients in a timely manner and document process appropriately
  Job Types: Full-time, Contract
  Pay: $1,784.00 - $2,120.04 per week

Benefits:

• Referral program

Experience:

• Registered Nurse: 2 years (Required)
• Clinical research: 2 years (Required)

License/Certification:

• BLS Certification (Required)

Work Location: On the roa