ZipRecruiter

Log In

1

Biomarker Operations Jobs in San Ramon, CA (NOW HIRING)

Predicine

Sr. Bioinformatics Scientist - CDSDM

Hayward, CA · On-site

$140 - $190/hr

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 ...

Exelixis

Sr Director, Biostatistics

Alameda, CA · On-site

Sets direction for statistical support of translational medicine and clinical biomarkers ... Has functional understanding of other disciplines such as data management, clinical operations ...

Exelixis Inc

Sr Director, Biostatistics

Alameda, CA · On-site

$248 - $352.50/hr

Sets direction for statistical support of translational medicine and clinical biomarkers ... Functional understanding of other disciplines such as data management, clinical operations ...

Exelixis

Sr Director, Biostatistics

Alameda, CA · On-site

Sets direction for statistical support of translational medicine and clinical biomarkers ... Has functional understanding of other disciplines such as data management, clinical operations ...

Exelixis

Sr Director, Biostatistics

Alameda, CA · On-site

Sets direction for statistical support of translational medicine and clinical biomarkers ... Has functional understanding of other disciplines such as data management, clinical operations ...

F. Hoffmann-La Roche Ltd

Senior Scientist

Pleasanton, CA · On-site

$101K - $138K/yr

Analyze biomarker expression patterns across tissues, cell types, and tumor models to ensure ... Collaborate cross-functionally with R&D, pathology, operation, and regulatory teams. * Contribute ...

Roche

Senior Scientist

Pleasanton, CA · On-site

$101K - $139K/yr

Analyze biomarker expression patterns across tissues, cell types, and tumor models to ensure ... Collaborate cross-functionally with R&D, pathology, operation, and regulatory teams. * Contribute ...

Gilead

Exec Director, Regulatory Affairs

Foster City, CA · On-site

$174K - $230K/yr

... of biomarkers in clinical studies. You will provide operational and technical regulatory assistance through all stages of clinical development through global registration for IVD projects. In ...

previous page

Showing results 41-60

All JobsBiomarker Operations JobsBiomarker Operations Jobs in San Ramon, CA

Biomarker Operations information

See San Ramon, CA salary details

$12

$29

$59

How much do biomarker operations jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for biomarker operations in San Ramon, CA is $29.33, according to ZipRecruiter salary data. Most workers in this role earn between $19.86 and $33.85 per hour, depending on experience, location, and employer.

What is biomarker operations?

Biomarker operations refer to the management and coordination of all activities related to biomarkers in clinical trials and research studies. This includes planning, collection, processing, analysis, and documentation of biological samples to ensure high-quality, reliable data. Professionals in biomarker operations work closely with clinical, laboratory, and data management teams to ensure compliance with protocols and regulations. Their work is essential for supporting drug development and personalized medicine initiatives.

What are the key skills and qualifications needed to thrive in biomarker operations?

To thrive in Biomarker Operations, you need a strong background in life sciences or related fields, experience with clinical research processes, and an understanding of biomarker development. Familiarity with laboratory information management systems (LIMS), data analysis tools, and regulatory compliance frameworks such as GCP is typically required. Excellent project management, organizational, and cross-functional communication skills are vital for coordinating between laboratories, clinical teams, and external partners. These competencies ensure the accurate, timely, and compliant execution of biomarker studies, which are critical for drug development and clinical decision-making.

What are some typical challenges faced in biomarker operations and how can they be managed?

Professionals in Biomarker Operations often encounter challenges such as coordinating complex sample logistics, ensuring data integrity across multiple sites, and managing tight timelines in clinical trials. Effective communication and collaboration with cross-functional teams like clinical operations, laboratory staff, and data management are essential to address these issues. Utilizing robust project management tools and maintaining clear documentation can help streamline processes and minimize errors, making it easier to navigate the dynamic and regulated environment of biomarker studies.

What are the most commonly searched types of Biomarker Operations jobs in San Ramon, CA?

The most popular types of Biomarker Operations jobs in San Ramon, CA are:

What job categories do people searching Biomarker Operations jobs in San Ramon, CA look for?

The top searched job categories for Biomarker Operations jobs in San Ramon, CA are:

What cities near San Ramon, CA are hiring for Biomarker Operations jobs?

Cities near San Ramon, CA with the most Biomarker Operations job openings:

Biomarker Operations jobs near you
Infographic showing various Biomarker Operations job openings in San Ramon, CA as of August 2026, with employment types broken down into 83% Full Time, 16% Part Time, and 1% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $61,004 per year, or $29.3 per hour.

Sr. Bioinformatics Scientist - CDSDM

Predicine, Inc

Hayward, CA • On-site

Full-time

Posted 17 days ago

Key responsibilities

  • Lead clinical study/trial data management and analysis, including data plans, integration, cleaning, reconciliation, QC, and analysis-ready dataset generation.

  • Develop and maintain clinical reporting, DTS/DTA, data transfer, ETL, and workflow automation tools for test and production data.

  • Define and maintain data specifications, data dictionaries, CRF/sample data requirements, validation documentation, and audit-ready records.

Job description

About Predicine

Predicine 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 Summary

We 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.

What You'll Do

Key Responsibilities & Time Allocation

% of TimeResponsibility30%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.


What You Bring

Education


MinimumPreferredLevelMaster's degree with 3+ years of relevant experienceDoctorate (PhD)Field of StudyBioinformatics, Biostatistics, Data Science, Computational Biology, Biomedical Informatics, Clinical Research, or related fieldSame fields

Experience


MinimumPreferredWork Experience2+ years in clinical study/trial data management, clinical reporting, DTS/data transfer, or biomarker analysisOncology 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, clinical data exchange, GCP/GCLP, CRFs, data dictionaries, validation, and study reporting
  • Strong attention to detail, data quality, reproducibility, compliance, and audit readiness
  • Excellent cross-functional communication skills

Preferred Skills & Qualifications

  • Experience with oncology diagnostics, NGS/biomarker data, clinical outcomes, or regulated clinical reporting
  • Pharma, biotech, CRO, central-lab, or clinical research industry experience
Join Us

At Predicine, you won't just manage data — you'll build the traceable, audit-ready foundation that makes cancer diagnostics and clinical trials trustworthy. If you're detail-driven, thrive on cross-functional collaboration, and want your work to directly support better patient outcomes, we want to hear from you.

Apply today and help us turn breakthrough science into better patient outcomes.

Predicine is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.