Software engineer
- Location
- San Francisco
- Type
- Full time
- Compensation
- $150k-$200k
- Posted
- 2 days ago
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The Clinical Informatics Programmer Specialist 4 applies advanced professional clinical informatics concepts and extensive knowledge of industry practices to projects of all levels of scope and complexity.
Involves the development and implementation of the organization's information systems and tools that are applied to clinical information. Works closely with clinicians across all hospital / healthcare departments to optimize effective use of systems. Coordinates analytical support for health management, including profiling, health economics, and business analytics / performance metrics. Defines systems and applications to support various functions. May provide customer service, troubleshooting and maintenance.
UCSF Health’s Genetics and Genomics Services, Clinical Cancer Genomics Lab (CCGL) and Genomics Medicine Lab (GML) aim to achieve the highest standards in patient care. The labs provides clinical genomics testing services in a wide variety of clinical areas with highly trained subspecialists who are recognized nationally and internationally for their expertise.
Required Qualifications:
Preferred Qualifications:
Education, Licenses/Certifications:
%
of time
Essential Function (Yes/No) Key Responsibilities50%YesSupport clinical operations of genetic testing laboratory throughgene curation, assessment of gene-disease correlation, and variant curation across the various genetic tests offered by the laboratory (e.g. hereditary cancer panel, exome, genome, and cancer gene panels).
Analyze clinical data selecting variants for curation/confirmation, variant nomenclature following HGVS guidelines.
Draft provisional medical reports for laboratory director review and sign out.
30%YesRoutine assessment of quality control metrics and , assisting with troubleshooting in collaboration with lab technicians and bioinformaticians as needed.
Track and manage the flow and analysis of patient data.
Develop and maintain databases of patient case status, human phenotype ontologies, and associated genetic analysis pipelines.
Ensure the handling of patient data is HIPAA and CLIA compliant.
Develop, maintain, and update local databases of clinical variant annotations relevant to human disease.
10%YesAid the laboratory directors and staff during the test development and validation of clinical testing pipelines.
Assist in the development of procedures and rules for classifying genetic variation according to ACMG/AMP guidelines, curation in internal databases, submission to ClinVar, and for publication.
Contributes to facilitating and promoting internal and external genomic projects by providing scientific or intellectual information.
5%Yes
Participate as a productive member of the work team and prepare cases for weekly team meetings.
Work with cross-functional teams, department, and providers on developing new tests, strategies to improve efficiency and accuracy for the GML/CCGL.
5%Yes
Assist in the instruction of trainees and training of new laboratory personnel.
Perform other related work as needed.
100%