Curation Scientist Step I
About Us
Founded in 2011, Fulgent has evolved into a premier, full-service genomic testing company built around a foundational technology platform.
Through our diverse testing menu, Fulgent is focused on transforming patient care in oncology, anatomic pathology, infectious and rare diseases, and reproductive health. We believe that by providing a wide range of effective, flexible testing options in conjunction with best-in-class service and support, we can redefine the way medicine is managed for patients and clinicians alike.
Since integrating with our therapeutic development business, Fulgent is also developing drug candidates for treating a broad range of cancers using a novel nanoencapsulation and targeted therapy platform. By merging our fields of expertise, we aim to become a fully integrated precision medicine company.
Summary of Position
This is the first step of the Genetic Curation Scientist career track. The Genetic Curation Scientist (GCS) Step 1 will be responsible for the classification of genetic variants following the ACMG guidelines (PMID: 25741868) and using a combination of internal proprietary software, published scientific literature, and publicly available databases. The GCS will determine the pathogenicity of DNA sequence variants found in real-time in patients and will customize clinical report text in collaboration with laboratory directors and genetic counselors. The GCS is also responsible for quality control, technical assessment, copy number analysis, and other interpretive components of molecular diagnostics as outlined in the curation standard operating procedures.
Key Job Elements
Perform quality control assessment for Next Generation Sequencing and other molecular diagnostic assays.
Classify detected variants according to internal and professional guidelines.
Draft clinical lab reports according to internal and professional standards; reports will be submitted to a laboratory director for final review and sign-out.
Review literature and databases to evaluate gene-disease association.
Review and update genetic variations based on new information.
Support the Client Services Department and Laboratory Genetic Counselors to respond to client requests for information on the interpretation of variants.
Participate in research & development projects as they arise.
Apply Now
Founded in 2011, Fulgent has evolved into a premier, full-service genomic testing company built around a foundational technology platform.
Through our diverse testing menu, Fulgent is focused on transforming patient care in oncology, anatomic pathology, infectious and rare diseases, and reproductive health. We believe that by providing a wide range of effective, flexible testing options in conjunction with best-in-class service and support, we can redefine the way medicine is managed for patients and clinicians alike.
Since integrating with our therapeutic development business, Fulgent is also developing drug candidates for treating a broad range of cancers using a novel nanoencapsulation and targeted therapy platform. By merging our fields of expertise, we aim to become a fully integrated precision medicine company.
Summary of Position
This is the first step of the Genetic Curation Scientist career track. The Genetic Curation Scientist (GCS) Step 1 will be responsible for the classification of genetic variants following the ACMG guidelines (PMID: 25741868) and using a combination of internal proprietary software, published scientific literature, and publicly available databases. The GCS will determine the pathogenicity of DNA sequence variants found in real-time in patients and will customize clinical report text in collaboration with laboratory directors and genetic counselors. The GCS is also responsible for quality control, technical assessment, copy number analysis, and other interpretive components of molecular diagnostics as outlined in the curation standard operating procedures.
Key Job Elements
Perform quality control assessment for Next Generation Sequencing and other molecular diagnostic assays.
Classify detected variants according to internal and professional guidelines.
Draft clinical lab reports according to internal and professional standards; reports will be submitted to a laboratory director for final review and sign-out.
Review literature and databases to evaluate gene-disease association.
Review and update genetic variations based on new information.
Support the Client Services Department and Laboratory Genetic Counselors to respond to client requests for information on the interpretation of variants.
Participate in research & development projects as they arise.
Apply Now