Clinical Genomic Scientist- Clinical Indication
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Baylor Genetics
US
Summary
The Clinical Genomics Scientist is responsible for curating variants and genes following ACMG guidelines and analyzing complex clinical genomics data. They also draft clinical reports and assist in the validation of new technologies and software platforms.
Job Description
Summary:
Baylor Genetics, one of the world leaders in clinical molecular genetics, is excited to announce an opening in the Clinical Genomics Interpretation (CGI) division. This role requires a comprehensive understanding of clinical genetics, familiarity with reviewing clinical notes, and ability to interpret a pedigree.
As part of the WGS Clinical Indication Team, the “Clinical Genomic Scientist” reviews clinical notes and converts patient phenotypes into Human Phenotype Ontology (HPO) terminology, records prior genetic testing history, interprets family history from pedigrees, and confirms consent answers from test requisition forms.
The Clinical Genomic Scientist 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 on the WGS Clinical Indication Team:
- 80 to 100%: Reviewing test requisition forms and clinical notes, extracting clinical information into structured data, such as HPO terms
- Up to 20%: As needed, opportunities for cross-training in WGS variant curations or WGS report writing may become available
Qualifications
- Degree: Master’s in Genetic Counseling, MD/PhD with a background in clinical genetics
- Preferred: Master’s in Genetic Counseling
Experience:
- 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).
- Desired: Experience in genetic counseling, familiarity reviewing clinical notes and medical writing.
- Desired: Familiarity with American College of Medical Genetics (ACMG) variant curation guidelines.
- Desired: Knowledge of genomic variation and its correlation with human disease.
Rank: Clinical Genomic Scientist – Clinical Indication I
- Degree: Masters in Genetic Counseling, MD, or PhD in clinical medicine, genetics, molecular biology, or equivalent.
- 0-1 years of experience with Human Phenotype Ontology (HPO)-related work and/or clinical experience.
Rank: Clinical Genomic Scientist – Clinical Indication II
- Degree: Masters in Genetic Counseling, MD, or PhD in clinical medicine, genetics, molecular biology, or equivalent.
- 2-4 years of experience with Human Phenotype Ontology (HPO)-related work and/or clinical experience.
Rank: Clinical Genomic Scientist – Clinical Indication III
- Degree: Masters in Genetic Counseling, MD, or PhD in clinical medicine, genetics, molecular biology, or equivalent.
- 4-6 years of experience with Human Phenotype Ontology (HPO)-related work and/or clinical experience.
- Thorough understanding of American College of Medical Genetics (ACMG) variant curation guidelines.
- Track record of high quality and leading projects toward goal
Rank: Clinical Genomic Scientist – Clinical Indication – Senior
- Degree: Masters in Genetic Counseling, MD, or PhD in clinical medicine, genetics, molecular biology, or equivalent.
- 4-6 years of experience with Human Phenotype Ontology (HPO)-related work and/or clinical experience.
- Thorough understanding of American College of Medical Genetics (ACMG) variant curation guidelines.
- Track record of high quality, leading projects toward goals, training coworkers, demonstration of workflow process improvement
Competencies:
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 dedicated to building an inclusive and diverse workforce. We do not discriminate based on race, religion, color, national origin, sex, sexual orientation, age, gender identity, veteran status, disability, genetic information, pregnancy, childbirth, or related medical conditions, or any other status protected under applicable federal, state, or local
Baylor Genetics is a leading diagnostic genomics partner offering a full spectrum of clinically relevant genetic testing, including Whole Genome Sequencing, Whole Exome Sequencing, and focused panels. Baylor Genetics combines rapid and comprehensive precision diagnostics options with the support of genetic counselors to help clinicians avoid a lengthy diagnostic odyssey for their patients, guide medical management, and ensure no patient with a genetic disorder gets left behind. Baylor Genetics’ testing menu covers family planning, pregnancy, neonatal and pediatric testing, oncology, and many other specialized testing options. Located in Houston’s Texas Medical Center, Baylor Genetics serves clients in 50 states.
Founded
1978
Company size
501-1,000 employees
Industry
Biotechnology Research
Org type
Privately Held
Headquarters
Houston, Texas
Baylor Genetics is a leading diagnostic genomics partner offering a full spectrum of clinically relevant genetic testing, including Whole Genome Sequencing, Whole Exome Sequencing, and focused panels. Baylor Genetics combines rapid and comprehensive precision diagnostics options with the support of genetic counselors to help clinicians avoid a lengthy diagnostic odyssey for their patients, guide medical management, and ensure no patient with a genetic disorder gets left behind. Baylor Genetics’ testing menu covers family planning, pregnancy, neonatal and pediatric testing, oncology, and many other specialized testing options. Located in Houston’s Texas Medical Center, Baylor Genetics serves clients in 50 states.
Founded
1978
Company size
501-1,000 employees
Industry
Biotechnology Research
Org type
Privately Held
Headquarters
Houston, Texas