Job Information
Providence St. Joseph Health Clinical Research RN in Seattle, Washington
Description Clinical Research RN @ Swedish First Hill Full time 8-Hour shift Relocation Assistance for eligible external candidates who meet all conditions for payment - this is in addition to the fantastic benefits and compensation package offered by Providence 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. Providence caregivers are not simply valued - they're invaluable. Join our team at Swedish Research 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. For direct patient care roles: Performs and maintains currency of essential competencies as required by specific area of hire and populations served. *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 Applications, study proposals and protocols as required. *Coordinates and supports interactions with third party payers as required. *Performs nursing duties within accepted standards of practice, including the Washington State RN Practice Act and established hospital policies and Standards. *Maintains current knowledge of nursing practice by attending continuing education, serving on hospital committees and/or completing unit-specific mandatory competency skills. *May transport investigational medications or devices. *Presents applicable clinical updates at staff meetings. Presents detailed clinical information to staff surrou