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Clinical Research Nurse Coordinator 1 - Women's
Clinical Research Nurse Coordinator 1 - Women'sInova Health System • Falls Church, VA, United States
Clinical Research Nurse Coordinator 1 - Women's

Clinical Research Nurse Coordinator 1 - Women's

Inova Health System • Falls Church, VA, United States
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Inova Fairfax Medical Campus is looking for a dedicated Clinical Research Nurse Coordinator 1 - Women's to join the team. This role will be PRN (4-6 shifts per month), nights; hours vary - typically 10 : 00 p.m. - 6 : 00 a.m.; must be flexible during training for a mix of day and night shift.

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 :

  • Retirement : Inova matches the first 5% of eligible contributions - starting on your first day.
  • 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.

Clinical Research Nurse Coordinator 1 - Women's 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 :

  • Education : BSN or AD. If RN has an AD, within six months from date of hire, they must meet with their nurse leader and conduct the following : 1.) Identify which accredited school they plan to attend 2.) Provide a written plan with anticipated BSN completion date 3.) Submit a review of transcripts from the school indicating the required pre-requisites and timeline for taking the courses 4.) Complete BSN within 24 months of start date.
  • Experience : 1 year of research training or protocol implementation
  • Certification : Basic Life Support from the American Heart Association Upon Start; Registered Nurse License Upon Start; Must be eligible to practice in VA
  • Preferred Qualifications :

  • Experience : L&D, C-section, and / or similar; research is a plus. Proficient in Spanish.
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    Clinical Research Coordinator • Falls Church, VA, United States

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