Government, Health Information Technology Provider, Private Industry
A patient presents with a cluster of clinical features that may have a genetic cause. The clinician accesses a suite of freely available, comprehensive, and authoritative online resources for genetic disease information to find answers. Navigating these integrated sources with ease and efficiency, she investigates potential genetic conditions associated with her patient’s clinical features, identifies reliable genetic tests she can order to make a diagnosis, and researches the genetic variants associated with the conditions. She also locates other actionable information, such as clinical guidelines, therapeutic approaches, and support for consumers. Her go-to resources have once again saved her hours of research and guesswork and helped her provide the best care for her patient.
These National Center for Biotechnology Information (NCBI) resources—ClinVar, MedGen, and the Genetic Testing Registry—aggregate data submitted by clinical laboratories and others worldwide, integrated from other authoritative sources through automated workflows, and curated by a team of staff. Together, they are changing the way clinicians investigate, diagnose, and manage inherited conditions. Computercraft is seeking a new member of the team to work on site at NCBI, National Institutes of Health, in Bethesda, Maryland, who will use his or her expertise in human genetics to advance these NCBI resources and NCBI’s Medical Genetics and Human Variation Program and contribute to data-sharing efforts for clinicians and researchers in the medical genetics community. The position will initially focus on ClinVar but is expected to broaden over time to address MedGen and the Genetic Testing Registry.
Evaluate and process submissions to ClinVar and other resources (e.g., data describing variants, diseases/phenotypes, interpretations, literature, supporting evidence)
Communicate with submitters to ensure accurate representation of the data
Engage with customers by email, phone, and video conferencing and in person
Collaborate with the team, including curatorial and technical development staff
Engage and educate users by contributing to public documentation
Review variant and disease/phenotype data
Ph.D. in human genetics with board certification in clinical or molecular genetics or M.S. in genetic counseling with ABGC or CBGC certification
Strong logic, problem-solving, and organizational skills
Excellent verbal and written communication skills
Excellent general computing skills, including familiarity with spreadsheets
Ability to work both independently and as part oPh.D. in human genetics with board certification in clinical or molecular genetics or M.S. in genetic counseling with ABGC or CBGC certificationf a team
Ability to balance multiple tasks in a fast-paced and dynamic environment
Ability to adhere to established procedures
A detail-oriented perspective
A strong desire to support public scientific databases such as ClinVar
Avid interest in genetic conditions and associated genomic causes
Other Desired Knowledge/Experience:
2+ years of experience with human variant interpretation in a clinical setting, either performing interpretation in a clinical testing laboratory or delivering interpretation results to patients
Comprehension of genetic condition phenotypes and familiarity with disease and phenotype databases
Understanding of the current "state of affairs" in the medical genetics community, including customer roles and needs from the clinic to testing laboratories, etc.
To apply for this position or learn about other Computercraft job opportunities, please visit the Careers section of our website: https://computercraft-usa.com/
Computercraft is an equal opportunity employer.
Additional Salary Information: Computercraft offers a competitive salary, excellent benefits package, the opportunity for excellent work-life balance with a standard 40-hour work week, and the chance to work with accomplished scientists at NIH/NCBI.
Internal Number: MGC0418
Computercraft, an American Indian– and Woman-owned small business established in 1981, provides the public with user-friendly access to reliable and current genetic sequence, genomic, chemical, and scientific information. Our technical and scientific staff work with customers to build and refine high-profile information resources that get accurate health and biomedical research data into the hands of researchers and other stakeholders all over the globe, helping them solve our world’s greatest health challenges.