Our bioinformatics team, working in biostatistics, genomics and bioinformatics in the next-generation sequencing (NGS) domain is expanding. We are searching for a bioinformatics data scientist to focus on design and improvement of PCR assays for high throughput NGS genomic sequencing. This exceptional opportunity offers the chance to work with a team focused on the forefront of genomic and cellular understanding of cancer.
Responsibilities:
- Work closely with software, experimental, regulatory, biological and clinical collaborators as a key member of the bioinformatics team in understanding assay performance
- Support the PCR primer/probe design. Identifies known and emerging nucleic acid biomarkers (SNV, InDel, DupDel, CNV, methylation, and fusions) via review of scientific papers and clinical trial summaries that drive treatment choices or are useful for monitor disease progression
- Analyze and interpret high-throughput internal DNA and RNA sequencing data from designed chemistry, with a specific focus on mutation identification and oncology characterization
- Improve biology/oncology understanding and assay performance based on the data.
Qualifications:
- MS with 3+ years of experience or PhD in genetics or related discipline
- Passionate about bioinformatics and data science
- Proven critical thinking capability with ability to follow through
- Proven understanding of both human genetics, oncology, and the genetic variation associated with various types of cancer
- Well versed with public sequence depositories of genome sequence and variation data, especially those focused on oncology and is able to query, retrieve, manipulate, and analyze data from these databases
- Experienced with the development of nucleic acid diagnostics based on the amplification of DNA and RNA via PCR
- Excellent communication (written and verbal) and data presentation skills.
Preferred:
- Deep knowledge and experience analyzing NGS data on human genome, either from industry or academia
- Proficiency with standard NGS tools like bwa, samtools, bedtools, etc.
- Experience working with somatic or low input DNA assays
- Experience and knowledge of commercially available of modern variant calling packages
- Proficient with excel or scripting language to analyze/understand NGS data
Pillar Biosciences aims to "Make precision medicine the first option for every patient" by developing and manufacturing targeted next-generation sequencing (NGS)-based assays and software for today’s high-throughput specialty NGS laboratories. We are seeking collaborative and independent problem solvers to support our mission.
Pillar Biosciences is an Equal Opportunity and Affirmative Action employer committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; religion; age; nationality; marital status; sexual orientation; disability or any other characteristic protected by law.
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What We Do
Pillar Biosciences was founded in 2014, on the principle that in order for personalized medicine to be realized, clinical Next Generation Sequencing (NGS) workflows need to be affordable, rapid, robust, and flexible. We’re focused on productive solutions that enable streamlined workflows, so that labs can generate dependable results with less inputs, less labor, and less time. Our team makes precision medicine practical through simple, efficient sequence enrichment technology and straightforward bioinformatics tools broadly available to molecular labs worldwide.
Why Work With Us
Our company was built on the foundational idea that a more collaborative approach to clinical NGS can help make precision medicine accessible for a wider range of laboratories. Join us if you're looking to join the genomic revolution in the clinical testing marketing and you want your ideas and contributions to have a significant impact.
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