Registered Nurse

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Registered Nurse

Quick overview

The Registered Nurse is responsible for conducting clinical trial visits, including physical assessments, specimen collection, and medication administration. They must ensure all activities are performed according to ICH/GCP guidelines and handle post-visit data submissions.

Requirements summary

Candidates must be an experienced Registered Nurse with an active, unencumbered license and a preference for clinical research experience. Strong organizational skills, technology proficiency, and the ability to travel locally or across state lines are required.

professional certificateMedication AdministrationPatient CommunicationVenipunctureVital Signs MonitoringSpecimen CollectionPhysical AssessmentECGCentrifugingIV Catheter InsertionClinical Trial CoordinationICH/GCP CompliancePK Collection

Job description

Registered Nurse

Key Responsibilities

Complete onboarding and training requirements to perform clinical trial visits
Provide availability, confirm visit acceptance, communicate with clinical trial/program participant/patient
Prepare for the clinical trial visit by gathering supplies and equipment, testing the equipment, verifying expiration dates and determining visit readiness
Travel to location of clinical trial/program participant
Perform clinical trial visit activities within
RN scope of practice such as (but not limited to):
Physical Assessment
Venipuncture
PK Collection
Centrifuging, processing of blood, preparations for shipment
Medication or Investigational Medicinal Product administration/reconciliation ECG
Specimen collection
IV catheter insertion
Screenings
Questionnaires
Vital Signs, Height, Weight
Adverse events collection
Perform post visit data uploads/submissions as required
Communicate with project team for any issues with may arise or concerns during visit
Ensure clinical trial visit is conducted according to ICH/GCP and accuracy of data collected during the visit

Position Requirements

Experienced Registered Nurse (Adult, Pediatric, Neonatal) with active unencumbered license to practice
Experience and knowledge of working in clinical research trials preferred
Attention to detail and highly organized
Ability to prioritize and manage multiple tasks
Excellent verbal and written communication skills in English and the ability to complete detailed data
Ability to work independently and as part of a wider team
Technology savvy
Ability to travel locally or across states lines based on licensure