Sr. Clinical Genomic Scientist
Anywhere, United States
Job Description
The Clinical Genomics Scientist position is a remote work opportunity, with daily huddles, clear objectives, and flexible scheduling. Minimal on-site time at the headquarters in Houston, TX may be required. Come join our team from the comfort of your home office!
QUALIFICATIONS:
Education:
- Degree: PhD or MD level degree in clinical medicine, genetics, molecular biology, or an equivalent subject. Strong candidates with a Master’s degree and appropriate experience will be considered.
- Relevant experience: 4-7 years
- Certification (optional): MB(ASCP)
Experience:
- Knowledge of genomic variation and its relationship to human disease
- Knowledge of literature curation methodologies.
- Knowledge of variant detection, molecular mechanisms of disease, functional assays, and computational analysis.
- Technical expertise in clinical medicine, genetics, genomics, or molecular biology.
- Experience with data quality assessment.
- Excellent verbal and written communication skills.
- Proficiency in communicating an understanding of genetics details.
- Knowledge of principles and practices of data analysis as applied to experimental results.
- Experience in the application of ontologies for medical/biological annotation.
- An understanding of bioinformatics analysis to identify variants within genomic data sets, and variant effect prediction algorithms (desired).
- Experience with use of Perl, Python, or other programming language (desired).
- Ability to create scripts and process large quantities of data (desired).
DUTIES AND RESPONSIBILITIES:
- 50%: curation of variants, genes, and gene-disease correlations following ACMG guidelines, using our robust internal dataset, online resources, and published literature.
- 30%: analyzing clinical genomics data, including next-generation sequencing, Sanger sequencing, metabolomics, and chromosomal microarray.
- 10%: clinical report drafting.
- 10%: validation, process refinement, presenting findings at meetings, and performing other duties as needed.
- Adheres to Code of Conduct as outlined in the Baylor Genetics Compliance Program
- Performs other job-related duties as assigned.
PHYSICAL DEMANDS AND WORK ENVIRONMENT:
- Frequently required to sit
- Frequently required to stand
- Frequently required to utilize hand and finger dexterity
- Frequently required to talk or hear
- Frequently required to utilize visual acuity to operate equipment, read technical information, and/or use a keyboard
- Occasionally exposed to bloodborne and airborne pathogens or infectious materials
Apply
Career Focus: Analyst, Clinical Operations, Scientist
Similar Jobs
Genetic Counselor I
As a Genetic Counselor I, you will play a crucial role in our clinical s...
Vice President, Global Supply Chain
Scholar Rock is a biopharmaceutical company that discovers, develops, an...
Director Quality EMEA / Qualified...
Be a hero for our rare disease patients At Ultragenyx, we fundamentall...
Associate Director, Medical Writing (Clinical...
Be a hero for our rare disease patients At Ultragenyx, we fundamentall...