Clinical Genomic Scientist - WGS

Baylor Genetics; United States; On-site; USD 90,000 - 130,000; Full time

Job summary

Baylor Genetics is seeking a Clinical Genomic Scientist – WGS Review to play a central role in our cutting-edge whole genome sequencing operation. You will review clinical documentation, perform case analyses, and select variants relevant to the patient phenotype while collaborating with clinical reporting teams.

This position is fully remote and offers daily team huddles, clear objectives, and flexible scheduling.

Qualifications

• Degree: 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.

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; request confirmatory testing when necessary.
• Communicate findings at cross-team huddles.
• Opportunities for cross-training in WGS variant curations or clinical indication (HPO) may become available.

Skills

Genetics knowledge

Gene-disease correlation

Case analysis

Communication skills

Analytical thinking

Teamwork

Education

Master's in Genetic Counseling

MD or PhD in genetics or related field

Tools

Microsoft Office

Job description

Summary

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.

Summary

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.

Duties And Responsibilities On The WGS Analysis Team

80%, possibly up to 100%:

• 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

Up to 20%:

• As needed, opportunities for cross-training in WGS variant curations or clinical indication (HPO) may become available

Qualifications

For all ranks

• Degree: 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.

Rank: Clinical Genomic Scientist – WGS review I

• 1 year of prior experience with whole exome or whole genome case review is preferred

Rank: Clinical Genomic Scientist – WGS review II

• 2 years of experience with whole exome or whole genome case review is preferred

Rank: Clinical Genomic Scientist – WGS review III

• 5 years of experience with whole exome or whole genome case review is preferred

Rank: Clinical Genomic Scientist – WGS review – Senior

• 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

Rank: Clinical Genomic Scientist – WGS review – Professional

• 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

Experience And Competencies

• 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.

Physical Demands And Work Environment

• At your Home Office:
• Frequently required to sit, using screen, keyboard, and mouse.
• Punctuality attending virtual meetings
• Occasional weekend rotation may be needed (for example, once a month)

EEO STATEMENT

Baylor Genetics is proud to be an equal opportunity employer committed to fostering an inclusive and diverse workplace. We welcome and encourage applicants from all backgrounds to apply. We do not discriminate on the basis of race, color, religion, national origin, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, pregnancy, childbirth, or any other status protected by applicable federal, state, or local law. If you need an accommodation during the application process, please contact our Human Resources team.