Pediatric APRN/PA Research Clinician — Mon–Fri, No Nights

The Nemours Foundation; Wilmington (DE); Vor Ort; USD 110.000 - 140.000; Vollzeit

Zusammenfassung

The Nemours Foundation invites an APRN/PA to join its Clinical Research team at Nemours Children’s Hospital, Delaware. You will provide specialized medical care for patients aged 0–20 years participating in trials, operating Monday through Friday from 8:30 am to 5:00 pm with no nights or weekends.

You will coordinate and conduct trials, assist with IRB submissions, regulatory documents, patient recruitment, consent, data collection, and study monitoring.

Qualifikationen

• Graduate of an accredited Pediatric Nurse Program or an accredited Physician Assistant Program.
• Three years of related pediatric Advanced Practice clinical experience preferred.
• Current unrestricted APRN or PA license to practice in DE/PA; Pediatric NP Certification; BLS and PALS on hire.
• DE CSR, DE DEA, PA DEA; additional state licensure may be required.

Aufgaben

• Assess, diagnose, manage, and follow up with patients in Clinical Research projects.
• Document patient encounters with diagnoses, management, and follow-up plans.
• Identify patient/family needs and initiate referrals; provide teaching.
• Evaluate treatment compliance via calls, messages, and visits.
• Act as patient advocate and liaison; mentor junior coordinators.
• Utilize advanced nursing/PA practice per state laws and hospital policies.
• Coordinate with study staff; assist with IRB submissions and regulatory needs.

Kenntnisse

Interprofessional teamwork

Independent provider

Strong communication

Mentoring others

Ausbildung

Graduate Pediatric Nurse Program

Graduate PA Program

Jobbeschreibung

The Nemours Foundation invites an APRN/PA to join its Clinical Research team at Nemours Children’s Hospital, Delaware. You will provide specialized medical care for patients aged 0–20 years participating in trials, operating Monday through Friday from 8:30 am to 5:00 pm with no nights or weekends.

You will coordinate and conduct trials, assist with IRB submissions, regulatory documents, patient recruitment, consent, data collection, and study monitoring.