Sr. Bioinformatics Scientist – CDSDM
Listed on 2026-08-29
-
Research/Development
Data Scientist -
IT/Tech
Data Analyst, Data Scientist
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Sr. Bioinformatics Scientist – CDSDMFull Time Professional Hayward, CA, US
9 days ago Requisition
About PredicinePredicine Inc. is a precision oncology company advancing the fight against cancer through cutting‑edge genomic technologies and liquid biopsy solutions. We partner with pharmaceutical companies, clinicians, and researchers worldwide to bring next‑generation diagnostics from bench to bedside — faster, smarter, and more accessible. Join a team where your work directly impacts patient outcomes and the future of cancer care.
Position Overview:
The (Senior) Bioinformatics Scientist, Clinical Data Science and Data Management will support clinical studies and clinical trials through rigorous clinical data science and data management. This role integrates clinical, assay, biomarker, genomic, sample, and operational datasets into accurate, traceable, analysis‑ready data assets. The position emphasizes clinical study/trial data management, clinical reporting, data transfer specifications, data quality, validation, and reproducible outputs. At the senior level, the incumbent will lead cross‑functional data workflows from study setup through reporting, partnering with clinical, data management, biostatistics, regulatory, QA, project management, laboratory, and external stakeholders to ensure data integrity and audit‑readiness across the study lifecycle.
Job SummaryWe are seeking highly motivated individuals to support clinical studies and clinical trials through rigorous clinical data science and data management. The incumbent will integrate clinical, assay, biomarker, genomic, sample, and operational datasets into accurate, traceable, analysis‑ready data assets. The role emphasizes clinical study/trial data management, clinical reporting, data transfer specifications, data quality, validation, and reproducible outputs. For senior positions, the candidate will lead cross‑functional data workflows from study setup through reporting with clinical, data management, biostatistics, regulatory, QA, project management, laboratory, and external partners.
This is an exciting opportunity to join a fast‑growing startup, accelerate your growth, and make a positive, immediate impact on cancer diagnosis and treatment.
Key Responsibilities & Time Allocation
% of Time
Responsibility
30%
Clinical Data Management & Analysis — Lead clinical study/trial data management and analysis, including data plans, integration, cleaning, reconciliation, QC, and analysis‑ready dataset generation.
20%
Reporting & Workflow Tools — Develop and maintain clinical reporting, DTS/DTA, data transfer, ETL, and workflow automation tools for test and production data.
20%
Data Specifications & Documentation — Define and maintain data specifications, data dictionaries, CRF/sample data requirements, validation documentation, and audit‑ready records.
20%
Multi‑Source Data Integration — Integrate clinical metadata, assay results, NGS/biomarker data, sample tracking, and outcome data for study reporting and interpretation.
10%
Reporting & Stakeholder Deliverables — Generate reproducible tables, listings, figures, dashboards, reports, and written summaries for internal and external stakeholders.
Education
Minimum
Preferred
Level Master's degree with 3+ years of relevant experience Doctorate (PhD)
Field of Study Bioinformatics, Biostatistics, Data Science, Computational Biology, Biomedical Informatics, Clinical Research, or related field Same fields
Experience
Minimum
Preferred
Work Experience 2+ years in clinical study/trial data management, clinical reporting, DTS/data transfer, or biomarker analysis Oncology diagnostics, NGS/biomarker data, clinical outcomes, or regulated clinical reporting experience
Required Skills & Qualifications
- Strong R and/or Python data analysis skills; SQL, SAS, ETL, or workflow automation experience is a plus
- Hands‑on clinical study/trial data management, including cleaning, harmonization, QC, traceability, and documentation
- Familiarity with DTS/DTA,…
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