Hawthorne Health Inc

Pediatric Registered Nurse - Part Time, Contract

Posted on

November 8, 2025

Job Type

Contract

Role Type

Clinical Operations

License

RN

State License

New Jersey

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Help & Resources

Company Description

Hawthorne Health brings trials directly to investigators and patients in their communities by combining innovative technology with compassionate medical professionals, and we invite experienced healthcare experts to grow their careers by becoming part of the Hawthorne Hero network. Our Heroes are capable, motivated, and diverse - more importantly, they are dedicated to improving patients lives and the future of medicine for humanity.

Job Description

Requirements

Must be experienced in pediatric and infant blood draw 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

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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

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