Clinical Research RN

2 months ago


Seattle, United States Providence St. Joseph Health Full time

Description Clinical Research RN - Tumor Institute Research @ Swedish First Hill Full Time (40 Hour Week) Day Shift 8 Hour Shifts This position will be located at Swedish First Hill with occasional travel to other Swedish locations. Relocation for eligible external candidates who meet all conditions for payment - this is in addition to the fantastic benefits and compensation package offered by Providence Swedish that begin on your first day of employment. Join us, and find out how many ways we offer you the chance to focus on what really matters - our patients. Independently coordinates research and administrative tasks in support of one or more research studies across multiple locations and may require travel in your own vehicle. Works with study investigators and supervisor to address study-related issues. Backs up other coordinators as needed. Supports department financial performance through budgeting, billing and as directed. May develop specialized research instruments and assist in the preparation of scientific manuscripts or presentations. May entail regular after-hours support, occasional on-call work and occasional overnight business travel. Trains other research coordinators in the proper conduct of research studies and participates in quality control activities, as directed. Assists manager or supervisor in providing oversight of financial and quality initiatives. Provides clinical nursing care for privately, federally and/or commercially sponsored research activities. Ensure timely attention to and scheduling of clinical procedures required by research protocols for all patients enrolled on studies requiring such procedures. May supervise other research staff. Responsible for clinical education for study staff. Works cohesively within a team supporting a team approach to research. Providence caregivers are not simply valued - they're invaluable. Join our team at Swedish Research and thrive in our culture of patient-focused, whole-person care built on understanding, commitment, and mutual respect. Your voice matters here, because we know that to inspire and retain the best people, we must empower them. Supports research studies by performing site and study initiation with sponsors; data management including completion and submission of Case Report Forms; measuring and enforcing patient compliance to study procedures; participating in and supporting sponsor monitor visits and audits by federal regulatory agencies. Educates staff at clinics and hospital surrounding research protocols. Educates research staff and physicians regarding study requirements and patient status on trial. Sends out reminders to physicians and staff regarding study availability and eligibility criteria. Reviews charts to identify potential cases and consent patients for participation in study. Conducts clinical evaluations as required (i.e., screening visit, drug administration); educates patient and their family regarding study procedures; educates investigators, sub-investigators or other study staff regarding study content and status. Provides 24-hour on-call status for patients, investigators or other interested parties (if appropriate per specialty). Measures and monitors patient compliance to study requirements; creates source documents for data capture. Responds to sponsor requests for data queries; corrects errors in source data; and manages adverse events and home visits, if needed. Coordinates patient care throughout the entire study for all clinical and non-clinical procedures. Administers and monitors treatment protocols including: study procedures, management of side effects and drug accountability. Serves as communicator and liaison between: physicians, study monitors, staff, sponsors, peers, and administration. Actively participates in the preparation of publications, Investigational New Drug Appli



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