Senior Development Scientist at Freenome
Brisbane, California, USA -
Full Time


Start Date

Immediate

Expiry Date

18 Oct, 25

Salary

216500.0

Posted On

19 Jul, 25

Experience

6 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

WHY JOIN FREENOME?

Freenome is a high-growth biotech company developing tests to detect cancer using a standard blood draw. To do this, Freenome uses a multiomics platform that combines tumor and non-tumor signals with machine learning to find cancer in its earliest, most-treatable stages.
Cancer is relentless. This is why Freenome is building the clinical, economic, and operational evidence to drive cancer screening and save lives. Our first screening test is for colorectal cancer (CRC) and advanced adenomas, and it’s just the beginning.
Founded in 2014, Freenome has ~400 employees and continues to grow to match the scope of our ambitions to provide access to better screening and earlier cancer detection.
At Freenome, we aim to impact patients by empowering everyone to prevent, detect, and treat their disease. This, together with our high-performing culture of respect and cross-collaboration, is what motivates us to make every day count.

Responsibilities
  • Design and execute studies to evaluate the impact of preanalytical variables (including blood collection, shipping, and storage conditions) on sample integrity, analyte stability, and performance impact on multiomic tests.
  • Identify preanalytical workflow and protocol improvements by analyzing and developing method data.
  • Design and lead the execution of verification and validation studies for IVD assays.
  • Collaborate with clinical laboratory members to transition development protocols into production, including automation, validation experiments, and SOP development.
  • Apply your knowledge of Design Control, Quality Management and Risk Mitigation to product and study design.
  • Document product development requirements and author study protocols and reports.
  • Work cross-functionally with internal teams (Program Management, Clinical Operations, Regulatory, Quality) and external vendors to plan and execute Development studies.
  • Collaborate with Computational Biologists and Biostatisticians to define data analysis approaches for Development and verification studies.
  • Mentor junior Scientists and Research Associates in the Preanalytical Development team in the design and execution of Development studies.
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