Clinical genomic scientist Job at Genome International Corp

Clinical Genomics Scientist, Oncology

BillionToOne is looking for a Clinical Genomics Scientist, Oncology to help driv...

Location

United States , Menlo Park

Salary:

158401.00 - 179521.00 USD / Year

BillionToOne

Expiration Date

Until further notice

Requirements

Ph.D. in Human Genetics, M.S. in Genetic Counseling, or related field
2+ years of experience in somatic variant interpretation based on ACMG/AMP guidelines in a clinical setting (alternatively, 1+ years of germline variant interpretation and 1+ years of somatic variant interpretation experience)
Hands-on experience working with human mutation databases (COSMIC, ClinVar, OncoKB), functional annotation sources (dbSNP), and genome browsers (UCSC)
Familiarity with IGV and BAM file analysis and data-minded willingness to learn to use basic bioinformatics tools, with technically minded insights
Knowledge of cancer somatic mutation and signaling pathways (e.g., which mutations have FDA approved drugs, Phase II/III clinical trials, which mutations are considered “hot targets” for drug development, etc.)
Exceptional attention to detail to follow highly detailed SOPs and strong organizational skills to track and manage clinical reporting and product improvement projects
Excellent communication skills and ability to work collaboratively with cross-functional teams
Operationally-defined flexible schedule, including weekends, as dictated by clinical reporting needs

Job Responsibility

Somatic variant interpretation and data review: Perform somatic-based variant interpretation, diving into the literature and databases to classify variants and match treatments for reporting, performing verification as required with BAM file analysis
Clinical report drafting: Carefully draft reports for each requisition primarily using in-house reporting API, working closely with the engineering and QA teams on reporting, and the laboratory directors on report language
Somatic mutation interpretation and reporting policy development: Work closely with lab directors, R&D, medical, and other related functions to develop and modify the somatic interpretation SOPs in accordance with ACMG/AMP guidelines, and the latest published literature
Content curation: Contribute to curation of gene-level content such as domain and critical residue curation
Molecular tumor board: Serve as a subject matter expert in consulting with the medical science liaison team, and presenting in molecular tumor boards to facilitate knowledge sharing
Contribute to oncology R&D: Work closely with the R&D team to help with somatic oncology based projects, providing expertise on variant interpretation, biological pathways/mechanisms, and other gene/variant-level reviews and analyses

What we offer

Working alongside brilliant, kind, passionate and dedicated colleagues, in an empowering environment, toward a global vision, striving for a future in which transformative molecular diagnostics can help millions of patients
Open, transparent culture that includes weekly Town Hall meetings
The ability to indirectly or directly change the lives of hundreds of thousands patients
Multiple medical benefit options
employee premiums paid 100% of select plans, dependents covered up to 80%
Extremely generous Family Bonding Leave for new parents (16 weeks, paid at 100%)
Supplemental fertility benefits coverage
Retirement savings program including a 4% Company match
Increase paid time off with increased tenure
Latest and greatest hardware (laptop, lab equipment, facilities)

Fulltime

Clinical Genomics Scientist, Prenatal

BillionToOne is seeking an experienced Clinical Genomics Scientist to support va...

Location

United States

Salary:

126721.00 - 147841.00 USD / Year

BillionToOne

Expiration Date

Until further notice

Requirements

Ph.D. in Human Genetics or a closely related field
Strong preference for candidates with experience in variant curation for carrier screening panels
Extensive experience in curating variants within CFTR, HBB, HBA1, and HBA2 is highly desirable
Proven ability to classify variants efficiently while maintaining accuracy within tight turnaround times

Job Responsibility

Germline Variant Curation: Conduct comprehensive reviews and classifications of newly identified variants, as well as reassess previously classified variants as needed
Curation Policy Development: Collaborate closely with clinical genomics scientists, laboratory directors, genetic counselors, and other stakeholders to develop and refine variant curation policies in alignment with industry best practices and society guidelines
Data Analysis & Interpretation: Leverage human mutation databases, functional annotation resources, and genomic browsers to facilitate accurate variant classification and reporting

What we offer

Working alongside brilliant, kind, passionate and dedicated colleagues, in an empowering environment, toward a global vision, striving for a future in which transformative molecular diagnostics can help millions of patients
Open, transparent culture that includes weekly Town Hall meetings
The ability to indirectly or directly change the lives of hundreds of thousands patients
Multiple medical benefit options
employee premiums paid 100% of select plans, dependents covered up to 80%
Extremely generous Family Bonding Leave for new parents (16 weeks, paid at 100%)
Supplemental fertility benefits coverage
Retirement savings program including a 4% Company match
Increase paid time off with increased tenure
Latest and greatest hardware (laptop, lab equipment, facilities)

Fulltime

Reporting Clinical Laboratory Scientist

The Prenatal Reporting Clinical Laboratory Scientist (RCLS) is responsible for p...

Location

United States , Union City

Salary:

126721.00 - 172625.00 USD / Year

BillionToOne

Expiration Date

Until further notice

Requirements

Must possess an active and valid CLS or Clinical Genetic Molecular Biologist Scientist (CGMBS) license issued by the state of California
Must fulfill requirements stated in 42 CFR 493.1489 OR 493.1491
Must fulfill requirements stated in the College of American Pathologists Molecular Pathology Checklist
Working knowledge of local, state, and federal laboratory regulations required
Bachelor’s degree or equivalent in Biomedical Laboratory Sciences, Clinical Science or related field required
At least one year of Clinical Laboratory experience or equivalent high complexity and volume laboratory experience required
Experience with molecular biology techniques required
Experience with Sanger sequencing analysis, trinucleotide repeat analysis, MLPA analysis, or NGS QC preferred
Laboratory experience in molecular biology within the last year preferred
Strong computer and automation skills are preferred

Job Responsibility

Clinical Data Review, Interpretation, and Reporting: Review and interpret clinical genomics data, and sign out clinical laboratory reports, ensuring accuracy and reliability of clinical reporting
Quality Assurance: Partner with Quality Management team on QC and QA programs to maintain the highest standards in laboratory testing and reporting, ensuring adherence to CLIA, CAP, and other regulatory guidelines
Process Improvement: Identify opportunities for process optimization, efficiency enhancement, and cost-effective laboratory practices
Collaborate with Research & Development, bioinformatics and Genomic Technology team to develop, validate, and implement of new laboratory tests, methodologies, and data management and reporting systems
Team Leadership: Provide leadership and guidance to laboratory staff, including scientists, technicians, and support personnel
Collaboration: Collaborate with cross-functional teams, including Lab Operation, Customer Service, Product, Commercial, to support company goals
Analysis and Reporting (70%): Execute the bioinformatics pipelines that process and analyze raw data from samples
Manage daily test processing needs with the highest emphasis on quality
Present sample results to additional RCLSs, Laboratory Director, and/or other clinical personnel for subsequent clinical reporting
Reviewing and releasing sample reports under the purview of the Laboratory Director

What we offer

Multiple medical benefit options
employee premiums paid 100% of select plans, dependents covered up to 80%
Extremely generous Family Bonding Leave for new parents (16 weeks, paid at 100%)
Supplemental fertility benefits coverage
Retirement savings program including a 4% Company match
Increase paid time off with increased tenure
Latest and greatest hardware (laptop, lab equipment, facilities)
Free daily on-site lunches provided from top eateries
A variety of perks on campus (state of the art gym, restaurant)
Free on-site EV charging (compatible with all EVs, including Tesla)

Fulltime

Scientist/Senior Scientist, Vascular

NewLimit is seeking an scientist with experience in endothelial biology to join ...

Location

United States , South San Francisco

Salary:

113000.00 - 171000.00 USD / Year

NewLimit

Expiration Date

Until further notice

Requirements

Ph.D. in cell biology, molecular biology, biochemistry or a related field or equivalent industry experience (5+ years)
Experience with primary endothelial cell isolation and functional characterization
Experience working with mouse models of endothelial cell function (e.g. kidney, cardiovascular, or cognitive disease models)
Experience with transgenic manipulation of endothelial cells either ex vivo or in vivo (e.g. using viral vectors, nucleic acid delivery)

Job Responsibility

Develop functional assays and pre-clinical models to measure endothelial cell function
Collaborate with our Functional Genomics and Predictive Modeling teams to test reprogramming hypotheses at scale
Measure the impact of mRNA reprogramming medicines on endothelial cell function
Engineer in vivo nucleic acid delivery methods for endothelial cells
Analyze and interpret experimental data to drive pre-clinical decision making

What we offer

Health, dental, and vision insurance
401(k) with company match
Paid parental leave
Industry-leading paid time off (PTO) — 20 days/year for all employees + holidays
Meals and snacks on-site

Fulltime

Research Engineer: Machine Learning for Computational Drug Discovery and Genomic Data Analysis

This is an opportunity to play a key role in the Accenture Labs BioInnovation te...

Location

Ireland , Dublin

Salary:

Not provided

Accenture

Expiration Date

Until further notice

Requirements

Design and implement AI research prototypes for the life sciences, including genomic medicine and computational chemistry
Collaborate with research scientists and engineers and turn experimental methods and their output into full-fledged prototypes to showcase the impact of our research
Develop and implement machine learning models for de novo molecule generation, property prediction
Design and optimize deep learning architectures (e.g., graph machine learning, transformers) for molecular optimization
Design and implements prototypes to learn insights from multi-omics data (e.g. genomics, transcriptomics, proteomics)
Build data ingestion pipelines to process and analyze large-scale biochemical and multi-omics datasets (e.g., SMILES, PDB, proteomics, genomics, clinical records)
Collaborate with subject matter experts to integrate domain knowledge into our AI models and interpret results
Stay on top of the latest advancements in AI/machine learning, AI for drug discovery, computational chemistry
Write clean, well-documented code

Fulltime

New

Senior Manager, Clinical Biomarker Operations

The Department of Research and Translational Medicine is seeking a Sr. Manager, ...

Location

United States , Boston

Salary:

160000.00 - 175000.00 USD / Year

Apogee Therapeutics

Expiration Date

Until further notice

Requirements

MS or higher with > 3 years or BS with >5 years of direct experience in biomarker operations role
Demonstrated experience with biomarker sample management, including sample logistics, reconciliation, and inventory maintenance from sample collection to long-term storage
Significant experience with CRO oversight, including contract management, SOW reviews, activity and accrual tracking, and final reconciliation of activities
Experienced in all phases of clinical trials, Phase 3 experience is an asset
Good understanding of biomarker assays, including flow cytometry, genomics, protein-based assays, and drug development in general
High level of emotional intelligence and able to collaborate effectively as a member of cross-functional teams, excellent communication skills to drive projects and manage timelines
Experience in I&I indications
Enjoys fast paced environment, flexible, able to manage multiple and competing priorities under tight timelines
Successfully exhibits Apogee’s C.O.R.E. values: Caring, Original, Resilient and Egoless
Ability and willingness to travel, including a minimum of ~4 times per year for All Hands meetings and other workshops

Job Responsibility

Plan, track, and manage logistics around biomarker sample collection across all our clinical trials, oversee sample shipments and testing at vendors, undertake sample reconciliation as needed, plan and inform teams on data delivery timelines, and manage final sample disposition
Ensure adherence to the clinical study protocol, contribute to biospecimen collection guidelines in protocols, ICFs, and lab manuals, and lead finalization of data transfer specifications
Maintain sample inventories, coordinate sample collection, and manage short-term and long-term sample storage solutions
Work in close collaboration with relevant stakeholders including Biomarker Scientists, Data Management, Clinical Operations, Legal, Finance, Procurement, and Quality Assurance
Support and coordinate review and finalization of MSAs, legal agreements, and other contracts related to clinical biomarker activities, labs, and partnerships
Support QA in vendor audit and inspection activities
Support activities related to biomarker budget planning and tracking of accruals
Lead vendor selection, performance management, and vendor oversight to ensure compliance with Apogee standards
Continuously identify and build best practices for process improvements
Ensure high quality data generation by overseeing sample integrity and external collaborations

What we offer

A great culture, grounded in our C.O.R.E. values: Caring, Original, Resilient and Egoless
Opportunity to work in a fast-paced, highly dynamic environment where you help shape the culture and company, wear multiple hats, and learn quickly
Market competitive compensation and benefits package, including base salary, performance bonus, equity grant opportunities, health, welfare & retirement benefits
We provide competitive time off, including three weeks PTO, two one-week company-wide shutdowns a year and dedicated paid sick leave
Commitment to growing you professionally and providing access to resources to further your development
Apogee offers regular all team, in-person meetings to build relationships and problem solve

Fulltime

Clinical Bioinformatics Scientist

Are you motivated to participate in a dynamic, multi-tasking environment? Do you...

Location

United Kingdom , Cambridge

Salary:

Not provided

NeoGenomics Laboratories

Expiration Date

Until further notice

Requirements

MSc or PhD in the field of computational biology, bioinformatics, or applied sciences, or significant industry experience in a relevant field required
2 years of bioinformatics experience in an academic or, preferred, industry setting
Solid understanding of NGS analysis
Scientific programming experience in R and/or Python (Essential)
Familiarity with data visualization libraries in R/Python such as ggplot2 or matplotlib (Essential)
Experience working in a UNIX environment (Essential)
Experience with or strong desire to learn next generation sequence data analysis (Essential)
Experience with cancer genomics data (Desired)
Experience with variant calling and exome/WGS pipelines (Desired)
Prior experience with work in a regulated environment, in particular for

Job Responsibility

Support the clinical team in analyzing data from clinical projects
Ensure samples are processed and results delivered within the target turnaround time (TAT)
Technical review of sequencing data
Perform non-standard assay processing of clinical samples
Lead data transfer activities
Attend, prepare and present material at international meetings of relevance, in alignment with company priorities
Lead exploratory data analysis to generate publishable material and/or inform R&D efforts regarding the current and future application of MRD assays
Follow all written procedures (SOPs) and safety requirements
Aid in the preparation of custom reports and analyses for collaborators

Fulltime

R&D Director

We are looking for a dynamic and visionary R&D Director who combines strategic l...

Location

Belgium , Kontich

Salary:

Not provided

Flen Health GmbH

Expiration Date

Until further notice

Requirements

Ph.D. in biopharmaceutical sciences, molecular biology, or a related discipline
Extensive experience in biopharmaceutical R&D, with a strong track record in wound healing and dermatology
Demonstrated hands-on expertise in functional genomics, structural and molecular biology, computational methods, and advanced skin and wound modelling
Proven success in leading and actively participating in teams and complex research projects
Strong publication and patent record in peer-reviewed journals, with direct contributions to scientific literature
Experience in securing and managing national and international research grants, including hands-on grant writing and project execution
Proven ability to lead international research consortia, delivering impactful outcomes through both strategic oversight and direct scientific involvement
Background in topical product development, with practical experience in formulation and testing

Job Responsibility

Provide both strategic direction and active, hands-on leadership to the R&D team, personally engaging in critical research activities and mentoring scientists at all levels
Lead by example in the discovery and development of new biopharmaceutical compounds, directly contributing expertise to projects targeting wound healing and skin inflammation
Build and strengthen the scientific evidence base for existing medical device products through direct involvement in experimental design, data analysis, and publication
Integrate disease insights with advanced pre-clinical methodologies, including functional genomics, structural and molecular biology, computational approaches, and both in vitro and in silico skin and wound models- by actively participating in experimental work and troubleshooting
Foster a culture of collaboration, innovation, and continuous improvement within the team by working side-by-side with team members and encouraging open scientific dialogue
Maintain a relentless focus on delivering value to patients and healthcare professionals ensuring that leadership decisions are grounded in practical, real-world impact
Establish and expand national and international research networks, leading projects and consortia that result in commercially viable innovative patents and products, including those supported by scientific grant programs

What we offer

Excellent working conditions
An innovative and inspiring work environment
Independent project work & responsibilities within a professional team
Career prospect
Learning and development opportunities
Flexible working ecosystem
Enthusiastic colleagues
Attractive remuneration package

Fulltime

Clinical genomic scientist

Genome International Corp

Location:

Category:
IT - Software Development

Contract Type:
Not provided

Salary:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
December 08, 2025

Looking for more opportunities? Search for other job offers that match your skills and interests.

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Clinical genomic scientist

Genome International Corp

Location:

Category:IT - Software Development

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Salary:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:December 08, 2025

Looking for more opportunities? Search for other job offers that match your skills and interests.

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Job Posted:
December 08, 2025