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2 jobs found in Aurora, CO

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Research Aurora, CO
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Dana-Farber Cancer Institute  (1) Professional Case Management  (1)
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Colorado  (2)
Professional Case Management
Jul 12, 2026
Part Time
RN Clinical Research - PRN
Professional Case Management Littleton, CO
Make a Difference on Your Own Schedule and Terms! Summary The Certified Mobile Research Nurse is a Registered Nursing per diem/PRN position for EmVenio. An EmVenio CMRN is responsible for setting appointments within the required visitation window to complete mobile visits for study participants. You'll work cooperatively with Clinical Project Managers, Coordinators, and site personnel to complete visits and submit accurate source documentation. We are looking for CMRNs to visit an Adult population who can perform the following skills during a mobile visit: Blood and urine specimen collection and processing IP receipt and return to courier at the visit Visits are to be completed M-F in the morning hours Required Qualifications Minimum of two (2) years of experience as a Registered Nurse (RN) Two (2) years' experience in starting and performing Phlebotomy/Peripheral Blood Draw, IVs, and Subcutaneous Injections (date of last practice within 6...
Nursing Research
Dana-Farber Cancer Institute
Jun 25, 2026
Full Time
Clinical Research Coordinator - Brighton
Dana-Farber Cancer Institute Brighton, CO
The Clinical Research Coordinator will work within the Brighton Dana-Farber Satellite clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator(s) and the DFCI disease programs. The Satellite CRC will be responsible for the primary data collection, management of patient clinical information, and regulatory documents as it pertains to participation in clinical trials across all studies open at the Satellite site(s). Ensures timely collection of protocol related samples including shipment to outside entities as required. Maintains site regulatory binders and ensures study compliance with all state, federal, and IRB requirements. May be responsible for site IRB submissions (violations, deviations, severe adverse event reports). This individual may also screen patients for protocol eligibility, obtain informed consent (minimal risk studies), and register study...
Research
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