Clinical Genomic Scientist- WGS Analysis

Baylor Genetics

1d • Remote

About The Position

The Clinical Genomic Scientist – WGS Review position has a central role in our
groundbreaking whole genome sequencing operation. This position involves
clinical documentation review, case analysis, candidate variant selection, and
collaboration with other clinical reporting teams. We seek candidates with a
strong understanding of gene-disease correlation, molecular mechanism,
inheritance, and evaluating the clinical relevance of genetic findings.

This position is fully remote and offers daily team huddles, clear objectives,
and flexible scheduling. Join our team and contribute to cutting-edge
genomics—from the comfort of your home office!

Why Baylor Genetics?

Work at the forefront of genomic medicine with a team of world-class
scientists.
Contribute to innovations that shape the future of personalized healthcare.
Enjoy a collaborative environment that values expertise, growth, and impact.

Requirements

• Masters in Genetic Counseling, MD, or PhD in clinical medicine, genetics, molecular biology, or equivalent.
• Familiarity with American College of Medical Genetics (ACMG) variant curation guidelines.
• Expertise in concepts of clinical medicine, genetics, genomics, and molecular biology.
• Knowledge of genomic variation and its correlation with human disease.
• Familiarity with American College of Medical Genetics (ACMG) variant curation guidelines.
• Experience in communicating genetic details effectively.
• Proficiency in Microsoft Office (Excel, Word, PowerPoint, Outlook).
• Competencies include Quality Assurance, Analytical and Problem-Solving Skills, Technical Skills, Interpersonal Skills, Oral and Written Communication, Teamwork, Organizational Support, Safety and Security, Dependability, Innovation, Adaptability.

Nice To Haves

• 1 year of prior experience with whole exome or whole genome case review is preferred
• 2 years of experience with whole exome or whole genome case review is preferred
• 5 years of experience with whole exome or whole genome case review is preferred
• 7 years of experience with whole exome or whole genome case review is preferred Demonstration of thorough expertise of gene-disease correlation, case analysis variant selection
• 10 years of experience with whole exome or whole genome case review is preferred Demonstration of thorough expertise of gene-disease correlation, case analysis variant selection Track record of high quality, leading projects toward goals, training coworkers, demonstration of workflow process improvement

Responsibilities

• Review test requisition forms and clinical notes; perform case analysis using the Emedgene platform; identify and select variants relevant to the proband’s phenotype; and request confirmatory testing when necessary.
• Communicate findings at cross-team huddles
• As needed, opportunities for cross-training in WGS variant curations or clinical indication (HPO) may become available

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: Ph.D. or professional degree