Clinical Research Nurse Coordinator 1 - Women's

Clinical Research Nurse Coordinator 1 - Women's

Inova Fairfax Medical Campus is looking for a dedicated Clinical Research Nurse Coordinator 1 - Women's to join the team. This role will be part-time (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:

• 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.
• 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 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.