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Posted: 06-Jan-26
Location: Phoenix, Arizona
Type: Full Time
Internal Number: 987446
Position Summary
The role operates on a primarily Monday-Friday day shift (approximately 9:00 a.m.-5:00 p.m.) with flexibility based on clinical reporting needs and follows a hybrid work model combining on-site and remote work. There is no patient interaction. The ideal candidate brings experience in clinical variant interpretation within a CAP/CLIA environment, strong scientific judgment, and the ability to communicate complex genomic findings clearly and effectively. This position reports to laboratory leadership within a small, multidisciplinary team and is evaluated on turnaround time, report productivity, regulatory compliance, collaboration, and contributions to continuous improvement. Competitive compensation is offered, with flexibility for sign-on bonuses, relocation, and remote work options based on qualifications and experience
The Clinical Genomic Scientist is a newly created role supporting the expansion of clinical genomic services within a growing pediatric laboratory. This position is responsible for clinical variant interpretation, classification, and reporting for next-generation sequencing-based testing, including NGS panels, whole exome sequencing, and whole genome sequencing. Working closely with Medical Directors, Genetic Counselors, and laboratory partners, the scientist applies established clinical guidelines to deliver accurate, high-quality, and clinically actionable genomic results while supporting assay development, validation, and the adoption of emerging genomic technologies
The Clinical Genomics Scientist plays a critical role in variant interpretation, classification, and reporting to support clinical genomic testing. This position provides high-level scientific expertise in the analysis of genetic testing data including next-generation sequencing (NGS) such including NGS panels, whole exome sequencing (WES), and whole genome sequencing (WGS). The scientist will collaborate with be working closely with laboratory director to ensure high-quality, clinically reliable genomic results.
This role also plays a key part in supporting the growth and development of Phoenix Children’s Clinical Genomics Laboratory and in integrating emerging genomic technologies. The individual will work closely with the Medical Director of Clinical Genomics to advance the adoption of cutting-edge innovations in this rapidly evolving field, ensuring that Phoenix Children’s remains at the forefront of genomic testing. Responsibilities also include supporting the director’s efforts in test development, implementation, optimization, and validation.
Education
- PhD or Master’s degree in Genomics, Molecular Biology, or related field. (Required)
- Coursework or certification in Human Genetics or Molecular Diagnostics. (Preferred)
- Continuing education in Clinical Genomics or Molecular Pathology. (Preferred)
- CLIA/CAP regulatory training or equivalent laboratory coursework. (Preferred)
- Demonstrated professional or scholarly involvement in genomics. (Preferred)
Experience
- 3 or more years experience in Clinical Genomics or Molecular Diagnostics. (Required)
- Proficiency in variant interpretation and tertiary analysis software. (Required)
- Knowledge of ACMG/AMP classification and clinical reporting. (Required)
- Experience with gene curation, panel development, or workflow validation. (Preferred)
- Experience in a CLIA/CAP-accredited laboratory. (Preferred)
Special Skills
- Strong knowledge of molecular genetics and variant databases. (Required)
- Proficiency with bioinformatics and tertiary analysis tools. (Required)
- Effective written and verbal communication skills for clinical collaboration. (Required)
- Analytical and problem-solving skills for complex data interpretation . (Required)
- Basic scripting or coding knowledge to interface with bioinformatics workflows. (Preferred)