Senior Research Associate (Contractor)

Freenome • Brisbane, CA

8h • Onsite

About The Position

At Freenome, we are seeking a Senior Research Associate to help grow our Genomics Assay Development team. At Freenome, you will help develop the assay technologies used to analyze patient samples and contribute to our mission of early cancer detection. The ideal candidate will work to develop assay technologies for our multiomic platform manually and on robotic platforms. You will develop, characterize, verify, and validate clinical-grade assays to measure complex, blood-based analytes (e.g., whole-genome sequencing of cfDNA). You will work cross-functionally with Research & Development teams, automation and process engineering, computational science, and clinical operations to develop and transfer NGS-based assays in a regulated, high-throughput environment. You are passionate about developing life saving diagnostics using NGS technologies, and you will have a significant impact on the continued growth of an organization dedicated to changing the entire landscape of cancer.
The role reports to the Manager of Genomics Late Stage Development. This role will be an onsite role based in our Brisbane, California headquarters.

Requirements

• Bachelor’s or Master’s degree in molecular biology, biochemistry, genetics, or a related field with at least 4 years of professional experience in the life sciences.
• Experience executing verification and validation studies for IVD assays in a regulated laboratory environment (GLP)
• Hands-on experience in Next-gen sequencing (NGS) based assay development including extraction, library preparation, target capture, and sequencing
• Familiarity with molecular biology, genomics, NGS, assay development, sample preparation, reagent handling, or related laboratory workflows (e.g. plasma separation processes, DNA/RNA extraction, purification, and quantification, NGS library preparation)
• Experience designing, planning, and executing successful experiments, interpreting results, preparing data for review, and giving effective scientific presentations
• High attention to detail and ability to record accurate and detailed observations, assess impact, and perform troubleshooting as required
• Ability to manually pipette with high confidence, accuracy, and precision
• Clear and proactive communication skills and ability to collaborate effectively with team members in the same and adjacent disciplines
• Strong organizational skills and the ability to contribute the design and implementation of new processes
• Flexible and highly motivated to learn new skills and comfortable adapting to changing priorities

Nice To Haves

• Prior experience in clinical diagnostics and/or working in a start-up environment is preferred
• Experience in working with with methylated ctDNA/cfDNA as an analyte in liquid biopsy workflows
• Experience with automated liquid handlers, laboratory information systems, sample tracking systems, and equipment scheduling/status tools
• Familiarity with programing in a scientific programming language (e.g., Python or R)

Responsibilities

• Apply knowledge of molecular biology, nucleic-acid biochemistry, and next-generation sequencing to develop assays for DNA, including genome-wide and targeted approaches
• Participate in experimental design and independently plan and execute mission-critical experiments to optimize and characterize assay performance
• Create and manipulate high impact assay inputs, including use of biological samples and formulation of contrived samples and reagents as required
• Gather high-quality data, take detailed notes, and openly communicate on lessons learned while performing experiments
• Perform data analysis, create summary presentations, and present results cross-functionally
• Perform technical troubleshooting, identify and implement process improvements across the lab by thinking critically about the execution of all experiments
• Build productive working relationships and collaborate with engineers and clinical laboratory members to transition development protocols into clinical production, including automation, validation experiments, and SOP development
• Contribute to writing study protocols and reports. Diligently apply current Good Laboratory and Documentation Practices (cGLP, cGDP)

Benefits

• Contractors may be hired through a third-party provider and will be considered contingent workers.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior