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Biomarker Data Manager Jobs (NOW HIRING)

Agilent

The Clinical Data Manager will plan and oversee all data management activities across assigned ... Direct experience supporting oncology clinical trials, biomarker-driven studies, companion ...

Bristol-Myers Squibb Company

Senior Manager

Princeton, NJ · On-site

$91K - $112K/yr

Execute data science and biomarker analyses on datasets from BMS clinical trials and real-world ... Manage and coordinate resources to produce quality deliverables within timelines for competing ...

Bristol Myers Squibb

Senior Manager

Princeton, NJ

$91K - $112K/yr

Execute data science and biomarker analyses on datasets from BMS clinical trials and real-world ... Manage and coordinate resources to produce quality deliverables within timelines for competing ...

Artech Information System LLC

Data Architect

Pennington, NJ

$64.25 - $82.75/hr

This includes FLOW Cytometry biomarkers data integration and visualization for Translational ... Working knowledge of software development life cycles, configuration management and best software ...

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Biomarker Data Manager information

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$31K

$97.1K

$172K

How much do biomarker data manager jobs pay per year?

As of Aug 8, 2026, the average yearly pay for biomarker data manager in the United States is $97,145.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,000.00 and $125,500.00 per year, depending on experience, location, and employer.

What are some common challenges faced by biomarker data managers when handling multi-site clinical trial data?

Biomarker Data Managers often encounter challenges related to data consistency and standardization when aggregating results from multiple clinical trial sites. Differences in data collection methods, sample processing, and reporting standards can lead to discrepancies that must be carefully managed to ensure high-quality, reliable datasets. Collaborating closely with site coordinators, laboratory teams, and biostatisticians is crucial to resolve these issues. Implementing robust data validation protocols and frequent cross-site communications can help streamline the process and minimize errors.

What is a biomarker data manager?

Biomarker Data Managers are professionals who oversee the collection, management, and quality control of data related to biological markers (biomarkers) used in clinical research and drug development. They work closely with scientists, clinicians, and statisticians to ensure that biomarker data is accurately captured, stored, and analyzed according to regulatory standards. Their responsibilities also include designing data management plans, implementing data validation procedures, and ensuring data integrity throughout the lifecycle of clinical trials. This role is critical in supporting research that leads to new diagnostics and therapies.

What are the key skills and qualifications needed to thrive as a biomarker data manager?

To excel as a Biomarker Data Manager, you need a strong background in life sciences, data management, and clinical research, often supported by a degree in biology, biostatistics, or a related field. Familiarity with data management systems such as Medidata Rave, SAS programming, and regulatory compliance (e.g., GCP, CDISC) is typically required. Attention to detail, problem-solving skills, and effective communication are vital soft skills for ensuring data integrity and collaboration across research teams. These competencies are crucial for managing complex biomarker datasets accurately, supporting clinical decision-making, and meeting regulatory standards.

What is the difference between Biomarker Data Manager vs Biomarker Data Analyst?

AspectBiomarker Data ManagerBiomarker Data Analyst
CredentialsBachelor's or Master's in Life Sciences, Biostatistics, or related fields; experience with data management systemsBachelor's or Master's in Statistics, Data Science, or related fields; proficiency in data analysis tools
Work EnvironmentClinical research labs, pharmaceutical companies, biotech firmsResearch institutions, clinical trial teams, biotech companies
Primary ResponsibilitiesManaging biomarker data, ensuring data quality, maintaining databasesAnalyzing biomarker data, generating reports, statistical interpretation

The Biomarker Data Manager focuses on data collection, quality control, and database management, ensuring data integrity. In contrast, the Biomarker Data Analyst emphasizes analyzing data sets to derive insights and support research conclusions. Both roles require strong technical skills but differ in their core functions within the biomarker research process.

What cities are hiring for Biomarker Data Manager jobs? Cities with the most Biomarker Data Manager job openings:
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Biomarker Data Manager jobs near you
Infographic showing various Biomarker Data Manager job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $97,145 per year, or $46.7 per hour.

Associate Director, Clinical Data Management

Corcept Therapeutics

Redwood City, CA • On-site

$229K - $269K/yr

Full-time

Posted 10 days ago

Job description

The Associate Director, Clinical Data Management ensures optimized data collection, flow and access across EDC and non-EDC data sources. Responsible for accuracy, completeness and CDISC compliance of Corcept clinical databases.

 Responsibilities:

  • Works in cooperation with Director of Clinical Data Management to select and maintain preferred vendor network for data management activities
  • Reviews, proposes and obtains bids for tools enabling real-time data visualization, interrogation, and reporting
  • Manages strategic input into the design of data flow across EDC and non-EDC data sources across vendor network
  • Manages data management service providers to ensure the quality of deliverables and that timelines are met
  • Develops and contributes to the design of processes enabling near-real-time data access for Corcept clinical trials
  • Ensure data quality of clinical database through implementation of CDISC compliance
  • Reviews and critically assesses data query resolution metrics and suggests process improvement
  • Reviews study protocols to ensure that data collection and CRF design meet study objectives
  • Manages and oversees SAE reconciliation between clinical and pharmacovigilance database
  • Review clinical data for completeness, accuracy, and consistency in accordance with the investigational plan
  • Provide subject matter expertise to project team members during all phases of project life cycle
  • Provides accurate and timely clinical data to internal and external customers upon request
  • Manage development, test, and maintain data management systems
  • Manage development and periodic review of Data Management specific SOPs, WIs and templates
  • Provide subject matter expertise prior, during, and post internal and external audits and inspections
  • Maintain compliance with company and study-specific learning requirements

Preferred Skills, Qualifications or Technical Proficiencies:

  • Master's Degree in health care or life sciences preferred
  • Relational database experience, SQL, SAS, and clinical data management systems
  • Knowledge and experience with MedDRA, WHODrug and other Thesaurus classification of controlled management systems
  • Knowledge of CDISC/SDTM. Hands-on experience preferred
  • Hands-on experience working with mainstream EDC systems (e.g. Rave, Medrio, Inform)
  • Familiarity with Data Visualization Tools for quick customized data access (e.g Spotfire, Tableau, RShiny)
  • In-depth understanding of Data Management regulatory guidelines: ICH, GCDMP, 21CFR Part 11
  • Demonstrated strong management abilities for project and staff management of Data Management Deliverables in clinical development

Preferred Education and Experience:

  • Bachelors or higher in science, math or computer science
  • 10+ year experience in clinical trial industry (med device, pharma or biotech)
  • 10+ year experience in data management in clinical trial industry (med device, pharma or biotech)
  • Minimum of 3 years experience in preparing, executing, and finalizing Medical Coding (MedDRA and WHODrug) within the Medidata Rave Coder system
  • Strong knowledge of the MedDRA and WHODrug dictionaries along with their uprevisions
  • Experience in IT-related field a plus
  • Experience with Endocrinology clinical trials and CDISC therapeutic area standards
  • Experience with management of data flow and curation of biomarker data a plus
  • Experience managing Data Management CROs
  • Direct report management and oversight

The pay range that the Company reasonably expects to pay for this headquarters-based position is $229,300 - $269,800; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.

 Applicants must be currently authorized to work in the United States on a full-time basis.

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