Compensation:

$112,000-$120,000

Variant Scientist II (Development): REMOTE, USA

JOB OVERVIEW:

The primary responsibilities of this role include leading cross-functional projects to drive scientific innovation and excellence in variant classification, gene-disease validity, computational biology, and clinical data analytics. As a member of the Genomic Science Development team, the variant scientist will evaluate the latest scientific advancements to continuously improve the Ambry Classifi™ program and implement new analytical methods and automation tools. The successful candidate will focus on high impact data-driven outcomes to support business goals.

DUTIES AND RESPONSIBILITIES:

• Rigorous analysis of scientific data, whole genome sequencing results, evaluating external published literature and designing internal validation studies

• Leadership of cross-functional groups at the team, department, and enterprise level

• Demonstrate scientific expertise in molecular genetics, variant science, and gene-disease validity

• Develop innovative technologies, software tools, AI/ML to improve the quality and efficiency of variant, gene, disease, and clinical data curation and classification

• Develop robust processes to implement scientific advancements meeting all quality assurance standards and documentation requirements while maintaining operational efficiency

• Develop educational training modules and methods to ensure broad adoption of all scientific advancements in a high-throughput laboratory environment

EDUCATION AND KNOWLEDGE:

• Develop educational training modules and methods to ensure broad adoption of all scientific advancements in a high-throughput laboratory environment

TECHNICAL COMPETENCIES:

• Excellent written, verbal, and interpersonal communication skills to engage stakeholders and socialize success

• Ability to adapt to significant change that is inherent in development and innovation

• Ability to work in and contribute to a fast-paced, highly collaborative environment

EXPERIENCE:

• At least 3 years of experience in whole genome sequencing (WGS) case analysis and/or variant classification in either a commercial or clinical laboratory setting

• Post-doctoral fellowship preferred

• Experience in project, program, and change management preferred

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