Clinical Genomic Scientist- Clinical Indication
Baylor GeneticsUnited States
Posted December 8, 2025
Full Time
About the Company
Baylor Genetics is a leading diagnostic genomics partner headquartered in Houston’s Texas Medical Center, providing a comprehensive suite of clinically relevant genetic tests—including whole genome sequencing, whole exome sequencing, and targeted panels—to clinicians across all 50 states. Their services span family planning, pregnancy, neonatal and pediatric diagnostics, oncology, and rare disease evaluation, supported by rapid turnaround times and integrated genetic counseling. By combining state‑of‑the‑art sequencing technology with expert genetic counselors, Baylor Genetics helps clinicians shorten diagnostic odysseys, guide precision medical management, and ensure that no patient with a genetic disorder is overlooked. The company’s commitment to accessibility, multidisciplinary support, and a broad testing menu distinguishes it as a trusted partner for precision medicine in the United States.
Job Description
Baylor Genetics is excited to announce an opening in the Clinical Genomics Interpretation (CGI) division for a Clinical Genomic Scientist. The role requires a comprehensive understanding of clinical genetics, familiarity with reviewing clinical notes, and ability to interpret a pedigree. The position is a remote work opportunity with daily huddles, clear objectives, and flexible scheduling.
Requirements
- Master's in Genetic Counseling, MD/PhD with a background in clinical genetics
- Expertise in concepts of clinical medicine, genetics, genomics, and molecular biology
- Experience in communicating genetic details effectively
- Excellence in reading/writing medical language
- Proficiency in Microsoft Office (Excel, Word, PowerPoint, Outlook)
- Familiarity with American College of Medical Genetics (ACMG) variant curation guidelines
- Knowledge of genomic variation and its correlation with human disease