Registered Nurse Research

Here is the formatted job description: **Registered Nurse - Research** **Location:** [City, State] **Schedule:** Monday - Friday, 7:00 AM - 4:00 PM **Job Type:** Travel, Full-time **Specialty:** Research, Clinical **Years of Experience:** 2 years **Duration:** 6 weeks **Project Details:** * Coordinate multiple research protocols and serve as a liaison with local investigators, clinical staff, and research personnel. * Practice and adhere to the "Code of Conduct" philosophy and "Mission and Value Statement". * Complete study medication order forms accurately, when needed, and have 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.). * 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.