Clinical Research Nurse Coordinator 1 - Womens

INOVA CmbHFalls Church, VA
2d

About The Position

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 (2-4 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.

Requirements

  • 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.
  • 1 year of research training or protocol implementation
  • Basic Life Support from the American Heart Association Upon Start
  • Registered Nurse License Upon Start
  • Must be eligible to practice in VA

Nice To Haves

  • L&D, C-section, and/or similar; research is a plus.
  • Proficient in Spanish.

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.

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.
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