Clinical Research Nurse Coordinator 1 - Neuroscience
Clinical Research Nurse Coordinator 1 - Neuroscience
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
Not Disclosed
Salary Not Disclosed
1 Vacancy
Job Description
Inova FairfaxHospital is looking for a dedicated Clinical Research Nurse Coordinator 1 Neuroscience to join the team. This role will be full-time Monday-Friday; regular business hours; 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:offeringup to $5250 per year in education assistance and up to $10000 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:offeringpaid time off paid parental leave & flexible work schedules.
Clinical Research Nurse Coordinator 1 Neuroscience 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 an RN has an AD within six months of the 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 the start date.
- Experience:1 year of research training or protocol implementation
- Certification:Registered Nurse Upon Start; Must be eligible to practice in VA; Basic Life Support from the American Heart Association
Preferred Qualifications:
- Experience:2 years of nursing research
- Education: Bachelors degree in Nursing
Required Experience:
IC
Employment Type
Full-Time
