TRAVEL - Research RN - Non Therapeutic Swedish (868) M-...

Details Client NameHCA HealthONE Swedish Job TypeTravel OfferingNursing ProfessionRN SpecialtyClinic Job ID30624645 Job TitleTRAVEL - Research RN - Non Therapeutic Swedish (868) M-F 7A-4P Weekly Pay$1964.45 Shift Details ShiftDay - 10x4 - 07AM Scheduled Hours40 Job Order Details Start Date02172025 End Date08042025 Duration24 Week(s) Job DescriptionJob Title: Research Nurse Job Specialty: Clinical Research Job Duration: 24 months Shift: 07:00-16:00 Guaranteed Hours: Not specified Experience: Minimum of 1 year License: Registered Nurse (RN) Certifications: Not specified Must-Have: Knowledge of research operations and regulations Job Description: - Coordinate multiple research protocols and serve as a liaison with local investigators, clinical staff, and research personnel. - Mature in understanding research operations and regulations to achieve a strong fundamental understanding of human subject research. - Adhere to the Code of Conduct philosophy and Mission and Value Statement. - Complete training assignments by the due date. - Accurately complete study medication order forms, obtaining necessary signatures before medication administration. - Perform routine operational activities for multiple research protocols. - Act as a liaison between site research personnel, industry sponsors, and supervisors. - Collaborate with various site departments, including finance, relevant hospital administrative representatives, and the local IRB, if applicable. - Coordinate protocol schedules from initial submission of feasibility until study closeout. - Obtain submission and approval for the Site's Facility Review Committee, if applicable. - Provide instruction on research protocols to staff, including interpretation of test results and study data to relevant personnel. - Assess patients and document findings at each clinic visit while on protocol. - Document specific tasks required by the protocol, such as medication forms, quality of life questionnaires, exams, and vital signs. - Ensure all medications are approved by appropriate designees before initiating treatment or changing medication regimens. - Accurately calculate and document BSA, creatinine, STS calculation, or any other conversions needed per protocol. - Record any interaction with patients while enrolled in a protocol, including follow-up and survival details. - Ensure follow-up appointments, imaging, or related procedures are scheduled according to protocol requirements. - Accurately complete and submit all data requests, including queries, within specified timeframes. - 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 managers. - Re-consent patients promptly and document processes appropriately. Client Details Address501 E Hampden Ave CityEnglewood StateCO Zip Code80113 Job Board DisclaimerBy applying for jobs on this website, you consent to receive daily messages from CYNET about assignments that match your profile. Email or text HELP for more info, or STOP to unsubscribe.Your mobile info will not be shared with third parties for marketing. Standard messaging and data rates may apply.

Created: 2025-02-21