Clinical Genomic Scientist- Clinical Indication

Baylor Genetics

$90K — $130K *
US-AnywhereRemote in United States
Healthcare
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • PhD or MD in clinical medicine, genetics, molecular biology, or equivalent.
  • 7+ years of relevant experience in clinical genomics.
  • Optional certification MB(ASCP).
  • Expertise in genomic variation and literature curation methodologies.
  • Proficient in variant detection, molecular disease mechanisms, and computational analysis.
  • Exceptional communication skills for conveying complex genetic information.
  • Experience in bioinformatics analysis and medical annotation ontologies.

Responsibilities

  • Lead variant curation and gene-disease correlation using extensive datasets and literature.
  • Conduct comprehensive analysis of clinical genomics data, including next-generation sequencing.
  • Draft and manage clinical reports and validation processes.
  • Present findings in team meetings, showcasing leadership in expertise.
  • Mentor and train junior staff, contributing to process improvement initiatives.

Benefits

  • Collaboration with a leading team of experts in clinical genomics.
  • Opportunity to shape research and practice through leadership roles.
  • Involvement in cutting-edge genomic technologies and methodologies.
  • Support for professional development and continuous learning.
Full Job Description
Job Summary

As a Senior Clinical Genomic Scientist, you will assume a leadership role in variant curation, data analysis, and interpretation in alignment with ACMG guidelines. This position significantly contributes to interpreting genomic data within clinical contexts, providing expertise, and guiding junior team members.

Qualifications and Experience:

  • Education:


  • Senior Clinical Genomic Scientist:


  • Degree: PhD or MD in clinical medicine, genetics, molecular biology, or equivalent.
  • Relevant Experience: 7+ years of demonstrated experience in the field.


  • Certification: Optional: MB(ASCP).


  • Profound knowledge of genomic variation, its impact on human diseases, and expert-level literature curation methodologies.


  • Mastery in variant detection, molecular disease mechanisms, functional assays, and computational analysis.


  • Technical expertise in clinical medicine, genetics, genomics, or molecular biology, coupled with extensive experience in data quality assessment.


  • Exceptional verbal and written communication skills, capable of conveying complex genetic information effectively.


  • Proficient in the application of ontologies for medical annotation and experienced in bioinformatics analysis for variant identification within genomic datasets.


Duties and Responsibilities:

  • 50%: Lead and oversee the curation of variants, genes, and gene-disease correlations following ACMG guidelines, utilizing extensive datasets, online resources, and published literature.


  • 30%: Perform comprehensive analysis of clinical genomics data involving various techniques such as next-generation sequencing, Sanger sequencing, metabolomics, and chromosomal microarray.


  • 10%: Draft clinical reports, manage validation processes, refine methodologies, and present findings in meetings, demonstrating leadership and expertise.


  • 10%: Provide mentorship, guidance, and training to junior team members, actively participating in process improvements and additional duties as needed.


PHYSICAL DEMANDS AND WORK ENVIRONMENT:

  • Frequently required to sit.


  • Frequently required to utilize hand and finger dexterity.


  • Frequently required to talk or hear.


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