Associate Director/Director, Computational Test Development

The Opportunity

We are seeking an Associate Director/Director-level computational scientist to drive the analytical and regulatory dimensions of diagnostic test development at Precede Biosciences. Reporting to the Senior Director of Computational Test Development, this role sits at the center of our effort to bring a novel epigenomics-based liquid biopsy platform from late-stage development through FDA regulatory submission.

You will lead the analytical strategy and bioinformatics infrastructure verification that underlies our validation programs. You will drive the interpretation of complex data, guide pipeline execution, and author critical regulatory documentation in close partnership with laboratory, clinical, and regulatory teams.

About Us

We are pioneering an advanced, minimally invasive, comprehensive epigenomics platform with the potential to profoundly impact the research and development of new medicines and the use of approved medicines in clinical practice across a number of conditions, including cancer. More information on our company and platform can be found on our company website and in our seminal publication in Nature Medicine.

What You'll Do

Analytical Validation & Regulatory Execution

• Design and develop computational approaches for characterizing the performance of existing and new epigenomic tests.
• Define and implement metrics and analyses to assess NGS and epigenomic data quality to enable coordinated optimization of assay and diagnostic performance.
• Lead the computational execution of verification and validation protocols, statistical analysis plans (SAPs), and performance summary reports to meet FDA evidentiary standards.
• Translate complex computational results into clear, well-organized regulatory documentation for FDA submissions.
• Stay current on FDA guidance for IVDs, companion diagnostics, and evolving LDT oversight to actively inform study design decisions.

Statistical & Bioinformatics Analysis

• Develop and apply statistical methods for diagnostic characterization, including LOD/LOQ, reproducibility, thresholding, guardbanding, and clinical utility endpoints.
• Support and optimize robust, reproducible analysis pipelines—ensuring code traceability and standardization from raw NGS data through regulatory-grade outputs.
• Identify and systematically address sources of variability, bias, and technical confounding across the computational workflow.

Cross-Functional Collaboration

• Partner closely with laboratory development, clinical operations, and regulatory affairs to ensure scientific and regulatory alignment across programs.
• Contribute to clinical study design—including sample size calculations, endpoint selection, and pre-specified SAPs using data-driven insights from analytical validation pilots.

What You'll Bring

• PhD in computational biology, bioinformatics, biostatistics, or a closely related quantitative field. Direct experience with advanced NGS modalities (e.g., cell-free DNA, ChIP-Seq, or epigenomic signal processing) is highly preferred.
• 4–9 years of industry experience in regulated diagnostics, liquid biopsy, or IVD development, ideally within a fast-paced, cross-functional R&D environment.
• Proven track record working under a formal Quality Management System (ISO 13485, 21 CFR Part 820).
• Hands-on experience contributing to regulatory submissions (such as Pre-Subs, De Novo, or 510(k) tracks).
• Solid grasp of analytical validation frameworks, including CLSI EP guidelines, FDA IVD/CDx guidance, and CAP/CLIA requirements.
• Fluency in R and/or Python for robust statistical modeling, data analysis, and reproducible reporting.
• Strong communication skills with a demonstrated ability to present and defend analytical validation strategies to internal leadership, scientific advisors, and regulatory stakeholders.
• Startup mindset: autonomous ownership of projects, adaptive under evolving information, effective in an entrepreneurial environment.

Compensation: $180,000 - $245,000 per year.