Registered Nurse

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 Screenings Vital Signs, Height, Weight Adverse events collection Perform post visit data uploads/submissions as required Communicate with project team for any issues that 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 state lines based on licensure Location This position requires RN travel to the location of the study/program participant/patient. Travel may be local or across state lines based on licensure to practice. #J-18808-Ljbffr