ABOUT FULGENT:

Fulgent is a leader in genetic and genomic clinical testing, a publicly traded company located in Los Angeles, California. We are a technology-driven company with extensive academic/clinical experience and capabilities in Next Generation Sequencing and bioinformatics. This distinction has advanced us to the forefront of the rapidly advancing genetic and genomic testing industry.

Fulgent's unique chemistries and superior proprietary bioinformatics pipeline has propelled our explosive growth in recent years. We offer the most expansive set of clinical genetic tests in the world, including molecular genetics (both germline and somatic), cytogenetics, FISH, IHC and flow cytometry. We are a CLIA and CAP accredited laboratory. Fulgent has state-of-the-art clinical, sequencing and bioinformatics tools, including the latest Illumina sequencers such as the NovaSeq.

SUMMARY OF POSITION:

The Lab Director is responsible for directing the overall function of the Fulgent Curation Department, including direct supervision of employees, sign out of somatic molecular genetics test results, and leadership in research & development. This position requires management skills that allow direct and indirect supervision of the curation scientist team to ensure our continuous quality, integrity, and efficiency of the curation process. Must be familiar and experienced in CAP, CLIA, and State and Federal regulations and certification standards and be responsible for ensuring full compliance of governing regulations. Due to the nature of our current test menu, significant experience with Somatic Next Generation Sequencing (NGS) in solid tumor profiling and/or heme NGS panels are required.

KEY JOB ELEMENTS:

• Final report sign-out of our patient reports.
• Provide leadership to the Operations, R&D, and Product Development teams in the areas of clinical and analytical validity.
• Lead curation team to work with research scientists and bioinformaticians on product development efforts.
• Collaborate with the software engineering team to design, optimize, and automate QC and data review interfaces.
• Design assay validation studies.
• Partner with quality management team to develop, implement and maintain SOPs and appropriate quality control and regulatory compliance programs.
• Work with technical supervisors to improve procedures for sequencing QC and data review, review sequencing quality indicators on a weekly basis, and help develop action plans.
• Refine curation protocols and classification criteria.
• Review variant classifications and final reports.
• Function as a knowledge resource for difficult cases.
• Develop new products in conjunction with the Genetic Counseling, Business Development, Sales, and Marketing teams.
• Assist with research, development, and grant applications with various teams including Business Development, Sequencing as a Service, and Research & Development.
• Be an ambassador to the genetics community, including giving public lectures, attending major conferences, and interacting with client providers such as physicians and Genetic Counselors.
• Author/co-author peer-reviewed scientific manuscripts.
• Other tasks as assigned.

QUALIFICATIONS:

KNOWLEDGE / EXPERIENCE:

• Have earned a PhD degree in molecular biology, genetics, or related field OR an MD degree with residency in Anatomic and/or Clinical Pathology (USA/Canada).
• ABMGG board-certified clinical molecular geneticist or board-certified molecular genetic pathologist.
• Required Experience with: (1) Interpreting variants in the context of the medical literature (especially experience with Somatic NGS testing), (2) Corresponding with medical geneticists and oncologists on the interpretation of results, (3) Design of gene panels and molecular tests, (4) Reviewing results of somatic NGS assays for validity, (5) CLIA lab operations and testing requirements.
• Comfortable in a fast-paced, dynamic team environment.
• Excellent leadership, human relations, and communication skills.
• Requires high attention to detail and the ability to multi-task and adapt rapidly to changing priorities and tasks.

SUPERVISORY RESPONSIBILITIES:

• Yes

REPORTS TO:

• Chief Scientific Officer

ENVIRONMENT:

Fulgent Therapeutics LLC is an Equal Employment Opportunity Employer.

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. The term "qualified individual with a disability" means an individual with a disability who, with or without reasonable accommodation, can perform the essential functions of the position.

For California residents, please see the link below to access our CCPA Privacy Notice.

https://tinyurl.com/FulgentCCPA