Baylor Genetics

Clinical Genomic Scientist- Carrier Screening

Analyzes clinical genetics data, curates variants and genes, and summarizes findings for clinical reports. Assists laboratory directors and R&D with validation of cutting-edge technologies and software platforms. This position offers remote work with daily huddles, clear objectives, and flexible scheduling.

Key Responsibilities
  • Curation (50%): curation of variants, genes, and gene-disease correlation following ACMG guidelines
  • Analysis (30%): analyzing clinical genomics data, selecting variants for curation/confirmation, variant nomenclature following HGVS guidelines
  • Other (20%): may involve clinical report drafting, test validation, process refinement, presenting findings, monitoring test turnaround time and task delegation
Required
  • Degree: PhD or MD in clinical medicine, genetics, molecular biology, or equivalent. Or strong candidates with a Master’s degree and relevant experience.
  • Familiarity with American College of Medical Genetics (ACMG) variant curation guidelines.
  • Knowledge of genomic variation and its correlation with human disease.
  • Expertise in concepts of clinical medicine, genetics, genomics, or molecular biology.
  • Experience in data quality assessment and communicating genetic details effectively.
  • Excellence in reading/writing medical language.
  • Proficiency in Microsoft Office (Excel, Word, PowerPoint, Outlook).
Preferred
  • Desired: MB(ASCP) certification.
  • Desired: experience in bioinformatics analysis, variant effect prediction algorithms, and scripting languages
 

Summary: 

The Clinical Genomics Scientist analyzes clinical genetics data, curates variants and genes, and summarizes findings for clinical reports. Our scientists assist laboratory directors and R&D with validation of cutting-edge technologies and software platforms.  

 

The Clinical Genomics Scientist I position is a remote work opportunity, with daily huddles, clear objectives, and flexible scheduling. Come join our team from the comfort of your home office! 

 

Duties and Responsibilities: 

  • Curation (50%): curation of variants, genes, and gene-disease correlation following ACMG guidelines 

  • Analysis (30%): analyzing clinical genomics data, selecting variants for curation/confirmation, variant nomenclature following HGVS guidelines 

  • Other (20%): may involve clinical report drafting, test validation, process refinement, presenting findings, monitoring test turnaround time and task delegation 

 

Qualifications/Experience 

  • Degree: PhD or MD in clinical medicine, genetics, molecular biology, or equivalent. Or strong candidates with a Master’s degree and relevant experience. Desired: MB(ASCP) certification 

  • Familiarity with American College of Medical Genetics (ACMG) variant curation guidelines. 

  • Knowledge of genomic variation and its correlation with human disease. 

  • Expertise in concepts of clinical medicine, genetics, genomics, or molecular biology. 

  • Experience in data quality assessment and communicating genetic details effectively.  

  • Excellence in reading/writing medical language.  

  • Proficiency in Microsoft Office (Excel, Word, PowerPoint, Outlook). 

  • Desired: experience in bioinformatics analysis, variant effect prediction algorithms, and scripting languages 

 

Competencies: 

Quality Assurance, Analytical, Problem Solving, 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) 

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