Clinical Research Nurse Coordinator 1 - Neuro Clinic
Inova Health System
Inova 8095 - Fairfax East (Inova Center for Personalized Health is looking for a dedicated Clinical Research Nurse Coordinator 1 – Neuro Clinic to join the team. This role will be full-time, Monday-Friday (regular office hours/flexible), no weekends or holidays. Inova is consistently ranked a national healthcare leader in safety, quality and patient experience. We are also proud to be consistently recognized as a top employer in both the D.C. metro area and the nation. Featured Benefits: * Committed to Team Member Health: offering medical, dental and vision coverage, and a robust team member wellness program. * Retirement: Inova matches the first 5% of eligible contributions – starting on your first day. * Tuition and Student Loan Assistance: offering up to $5,250 per year in education assistance and up to $10,000 for student loans. * Mental Health Support: offering all Inova team members, their spouses/partners, and their children 25 mental health coaching or therapy sessions, per person, per year, at no cost. * Work/Life Balance: offering paid time off, paid parental leave, & flexible work schedules.. Clinical Research Nurse Coordinator 1 Job Responsibilities: * Provides patient education and medical information to study patients to ensure understanding of proper medication dosage, administration, and disease treatment. * Delineates and defines the physiological status of the patient; assesses the educational, psychological and spiritual needs of the patient/significant other/family. * Administers investigational medications and performs patient assessments during clinic visits to determine the presence of side effects; notifies treating investigator of findings/issues. * Performs nursing duties as assigned and relevant to credentials and research study needs * Identifies and explains key protocol elements; performs study tasks under direct supervision. * Explains basic elements of subject safety including the reasoning behind the required use of an Institutional Review Board/Independent Ethics Committee, study activity documentation, and event reporting requirements. Demonstrates subject protection under direct supervision. * Explains the investigational products development process and identify key regulations to control these processes. * Explains and performs study operational activities in compliance with Good Clinical Practice (GCP) and non-GCP related study management activities. * Explains how to document data according to ALCOA-C (Attributable, Legible, Contemporaneous, Original, Accurate and Complete) principles. * Explains the importance of professional conduct and describe leadership principles that impact the effective operation of an investigative site. * Explains the variety of communication channels, roles and relationship and outlets for study results that impact the conduct of clinical research. * May perform other duties as assigned. Minimum Qualifications:
- Experience: 1 year of research training or protocol implementation
- Education: BSN or AD. If an RN has an AD, within six months of the date of
- Experience: Clinical experience as a Registered Nurse in neuro is a plus
- Education: Bachelor’s degree in Nursing
- Other: Must have confidence and awareness when speaking with patients and
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