ZipRecruiter

Log In

Sema4
Sema4

60 Sema4 Genomic Variant Scientist Jobs Hiring Near You

Mayo Foundation for Medical Education and Research

$88K - $132K/yr

Responsibilities The Variant Scientist functions in the clinical lab interpretive team, evaluating genomic test results to determine the pathogenicity and clinical significance of germline and ...

Washington University of St. Louis

$77K - $120K/yr

This position is focused on supporting clinical genomic testing workflows for the diagnosis of ... Focus of the position is on all aspects of genetic variant analysis, curation, and interpretation.

Baylor Genetics

The Clinical Genomics Scientist II analyzes clinical genetics data, curates variants and genes, and ... Familiarity with American College of Medical Genetics (ACMG) variant curation guidelines.

Baylor Genetics

Clinical Genomic Scientist - WGS

Summary: The Clinical Genomic Scientist - WGS Review position has a central role in our ... This position involves clinical documentation review, case analysis, candidate variant selection ...

next page

Showing results 1-20

All JobsSema4 JobsSema4 Genomic Variant Scientist Jobs

Variant Scientist III

Ann Arbor, MI • On-site

ThermoFisher Scientific
See more jobs at ThermoFisher Scientificexternal

Other

This job post has expired today. Applications are no longer accepted.

Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

Discover Impactful Work

The Variant Scientist III will review, analyze, and compile complex clinical data from primary literature and clinical trials specific to biomarkers in cancer. You'll provide scientific and technical expertise to a cross-functional team of scientists and software developers to build and maintain an internal knowledgebase of genomic aberrations and therapies relevant to cancer. This role is part of the Bioinformatics team within the Clinical Next Generation Sequencing Division. The mission of this business unit is to develop next-generation sequencing-based solutions to support oncology research and other important unmet medical needs.

Location

This is a fully onsite role based in Ann Arbor, MI and relocation assistance is not provided.

A Day in the Life

  • Read, interpret, and curate evidence from approved therapies, clinical guidelines, clinical trials, and scientific literature using customized software tools.

  • Actively participate in the interpretation, analysis, and summarization of various clinical sources for somatic and germline variant annotations and classification.

  • Review primary literature and author summaries that describe the relationships between gene variants and disease prognosis, diagnosis, and therapy selection.

  • Actively provide translational and clinical oncology expertise to the curation team in solid and/or hematological cancers.

  • Follow and maintain sustainable processes that ensure data accuracy and quality.

  • Work in a fast pace, cross-functional team of bioinformatics scientists, variant scientists, and software engineers to define and refine clinical reports.

Keys to Success Education
  • PhD in cancer biology, cancer genomics, or molecular biology with expertise in solid or heme cancers. Post-doctoral experience preferred but not required.
Experience

  • Demonstrated understanding of cancer genomics, tumor biology, oncogenic signaling pathways.

  • Experience in reviewing and summarizing scientific literature for somatic and germline variants.

  • Experience with cancer mutation databases and disease ontologies.

  • Industry or clinical laboratory experience working in genomic variant curation and clinical interpretation is preferred.

  • Experience with IVD/regulated product development or genetic counseling is a plus.

Knowledge, Skills, Abilities

  • Excellent written and oral communication skills.

  • Excellent organizational skills with ability to multi-task

  • Ability to work independently and collaboratively.

  • Positive attitude with strong interpersonal skills.

Other
  • Must be able to pass a comprehensive background check and drug screen.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

#J-18808-Ljbffr

Apply