Pediatric ARNP - Genetics

MultiCare Health System•Tacoma, WA

1d•$164,314 - $187,843•Onsite

About The Position

The Genetics Advanced Registered Nurse Practitioner (ARNP) delivers specialized genomic, metabolic, and genetic services for pediatric and adult patients and families. This role encompasses diagnostic assessment, genetic and metabolic testing coordination, infusion therapy administration, newborn screening follow-up, gene variant interpretation, and personalized management of inherited and metabolic conditions. Working closely with geneticists, metabolic specialists, genetic counselors, dieticians, and multidisciplinary teams, the ARNP ensures evidence-based care plans and seamless integration of precision medicine into clinical practice. The ARNP also leads program development and quality initiatives to advance health outcomes.

Requirements

Master's or Doctoral degree in Nursing (MSN or DNP) with a focus on genetics, pediatrics, or metabolic nursing
Current, unrestricted Washington State APRN license and Nurse Practitioner certification
National genetics nursing certification (e.g., ANCC Genomics Nursing Certification) certification preferred
Competency in infusion therapy protocols, infusion pump technology, and aseptic technique preferred
Familiarity with newborn screening programs, confirmatory testing guidelines, and early intervention services preferred
Basic Life Support (BLS) required
2 years of clinical experience in genetics, metabolic disease management, or infusion therapy preferred
Proficiency with Epic preferred
Strong analytical, diagnostic reasoning, and patient/family education skills

Nice To Haves

National genetics nursing certification (e.g., ANCC Genomics Nursing Certification)
Competency in infusion therapy protocols, infusion pump technology, and aseptic technique
Familiarity with newborn screening programs, confirmatory testing guidelines, and early intervention services
2 years of clinical experience in genetics, metabolic disease management, or infusion therapy
Proficiency with Epic

Responsibilities

Conduct comprehensive genetic and metabolic diagnostic assessments, pedigree analysis, and medical/family history reviews
Provide pre-test and post-test genetic counseling for inherited disorders, including inborn errors of metabolism
Coordinate and interpret genetic/genomic tests (panels, exome, genome) and metabolic assays (e.g., plasma amino acids, acylcarnitine profile)
Manage pharmacological, nutritional, and other therapeutic interventions, including infusion therapies for genetic and metabolic diseases in both outpatient and inpatient settings
Oversee newborn screening follow-up: review results, order confirmatory testing, initiate early interventions, and counsel families on outcomes
Document genetic and metabolic encounters, infusion orders, and newborn screening plans accurately in the electronic health record
Participate in developing and updating protocols for genetic and newborn screening workflows, informed consent, metabolic emergency plans, and infusion therapy
Monitor key metrics such as test turnaround time, infusion complication rates, dietary compliance, and newborn screening referral completion
Lead quality improvement projects to optimize metabolic crisis interventions, infusion therapy optimization, and patient education materials
Collaborate in case conferences and team meetings
Supervise and mentor genetic counseling interns, clinical trainees, nursing staff, and infusion teams on metabolic best practices
Embody organizational values of compassion, stewardship, collaboration, and respect
Adhere to hospital, departmental, and regulatory standards (e.g., HIPAA, CLIA, CAP, state newborn screening mandates)
Engage in departmental meetings, community outreach, newborn screening advocacy, and continuing professional development