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Cancer Data Management Jobs in Colorado (NOW HIRING)

Dana-Farber Cancer Institute

$26 - $34.50/hr

The Satellite CRC will be responsible for the primary data collection, management of patient ... We are united in our mission of conquering cancer, HIV/AIDS, and related diseases. We strive to ...

The US Oncology Network

Study Coordinator

Denver, CO

$60K - $75K/yr

Overview Rocky Mountain Cancer Centers, Colorado's largest and most comprehensive provider of ... Trials assigned will involve complex protocol management and assisting the data management ...

The US Oncology Network

Study Coordinator

Denver, CO · On-site

$60K - $75K/yr

Overview Rocky Mountain Cancer Centers, Colorado's largest and most comprehensive provider of ... Trials assigned will involve complex protocol management and assisting the data management ...

Owens & Minor

Senior Manager, Data Engineering

Denver, CO · On-site +1

$140K - $155K/yr

... Calm Health, Cancer Resources Services, and discount programs - all at no cost to you. * The ... Key Responsibilities Leadership & Team Management - Lead, mentor, and develop a team of data ...

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$32.6K

$102.1K

$180.9K

How much do cancer data management jobs pay per year?

As of Jul 18, 2026, the average yearly pay for cancer data management in Colorado is $102,149.00, according to ZipRecruiter salary data. Most workers in this role earn between $69,400.00 and $132,000.00 per year, depending on experience, location, and employer.

What are some typical daily responsibilities in a Cancer Data Management role?

In a Cancer Data Management position, your daily tasks often involve collecting, reviewing, and accurately entering patient oncology data into specialized cancer registries and databases. You’ll work closely with physicians, nurses, and other health professionals to verify clinical details, track patient outcomes, and ensure compliance with national reporting standards. Regular responsibilities may also include preparing statistical reports, conducting quality checks, and staying updated on changing data collection guidelines. This collaborative and detail-oriented work directly contributes to research, treatment planning, and institutional accreditation.

What is a Cancer Data Management job?

A Cancer Data Management job involves collecting, analyzing, and maintaining cancer-related data to support research, treatment, and prevention efforts. Professionals in this field, often called cancer registrars, ensure the accuracy and completeness of cancer patient records. They work with healthcare providers, researchers, and public health organizations to track cancer trends and outcomes. Their work plays a crucial role in improving patient care, guiding policy decisions, and advancing cancer research.

What is cancer data management job description?

A cancer data management professional is responsible for collecting, organizing, and maintaining accurate cancer-related data to support research, treatment, and outcomes analysis. They often use specialized software and adhere to data privacy standards, requiring attention to detail and knowledge of medical terminology and data systems. The role may involve collaboration with healthcare providers and researchers to ensure data quality and integrity.

How much does a cancer data manager make?

The average salary for a cancer data manager in the United States ranges from $60,000 to $85,000 annually, depending on experience, education, and location. In Texas, salaries tend to be within this range, with some positions offering higher compensation based on specialized skills and certifications such as data management or oncology-specific training.

What are the key skills and qualifications needed to thrive in the Cancer Data Management position, and why are they important?

Excelling in Cancer Data Management requires a background in health information management, data analysis, and familiarity with oncology terminology—often backed by a relevant degree or certified tumor registrar (CTR) credential. Expertise in specialized cancer registry software, electronic health records (EHRs), and regulatory reporting systems like SEER or NAACCR is commonly expected. Strong organizational skills, attention to detail, and effective communication are valuable for ensuring data accuracy and collaboration with clinical teams. These skills are vital to maintain high-quality data for cancer research, reporting, and patient care improvements.

Is cancer data management a good career?

Cancer data management is a specialized field involving organizing and analyzing cancer-related data to support research and patient care. It requires knowledge of healthcare data systems, attention to detail, and often familiarity with electronic health records and data privacy regulations. The role offers opportunities in healthcare, research institutions, and cancer centers with steady demand and potential for career growth.

How much do oncology data analysts make?

Oncology data analysts typically earn a median annual salary of around $60,000 to $80,000, depending on experience, education, and location. They often work with electronic health records and statistical tools to manage cancer-related data in healthcare settings.
What are popular job titles related to Cancer Data Management jobs in Colorado? For Cancer Data Management jobs in Colorado, the most frequently searched job titles are:
What job categories do people searching Cancer Data Management jobs in Colorado look for? The top searched job categories for Cancer Data Management jobs in Colorado are:
Cancer Data Management jobs near you
Infographic showing various Cancer Data Management job openings in Colorado as of July 2026, with employment types broken down into 1% Internship, 2% As Needed, 84% Full Time, 12% Part Time, and 1% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $102,149 per year, or $49.1 per hour.
Senior Director, Clinical Data Management

Senior Director, Clinical Data Management

Umoja Biopharma

Louisville, CO • On-site, Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 11 days ago

Job description

Umoja Biopharma is an industry-leading biotech with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. We are committed to our core values and principles that support our overall mission and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja to deliver on our goals. We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families.
Umoja Biopharma - Your Body. Your Hope. Your Cure.
POSITION SUMMARY
The Senior Director, Clinical Data Management will provide strategic and operational leadership for all clinical data management activities across Umoja's clinical development programs. This role sits within the Clinical organization and is accountable for ensuring the integrity, quality, and regulatory compliance of clinical trial data from protocol development through database lock and regulatory submission.
This individual will lead the planning, execution, and oversight of data management activities, clinical systems, and external vendors, while building scalable processes and capabilities to support a growing clinical pipeline. The role partners closely with Clinical Development, Clinical Operations, Biostatistics, Translational Medicine, Regulatory Affairs, and external partners like CROs to ensure timely delivery of high quality, decision-read-y- clinical data.
This role will be an Individual Contributor and will lead a matrixed team of vendors (CROs) and contractors to start. This person will be responsible for building out a future team.
This role will ideally be based in Seattle, WA or Louisville, CO but can be remote within the US. If remote, travel to Umoja Headquarters will be required at least once per quarter.
CORE ACCOUNTABILITIES
Specific Responsibilities include:Hands-On Clinical Data Management Execution (as needed while building CDM team)
  • Serve as the primary clinical data management lead for assigned clinical trials, with direct accountability for data quality, timeliness, and inspection readiness from protocol development through database lock.
  • Perform detailed protocol review with a focus on data flow, endpoints, data collection strategy, and facilitation of downstream analysis requirements.
  • Lead hands-on CRF design and review, ensuring alignment with protocol objectives-, statistical analysis plans, and regulatory expectations.
  • Develop, review, and approve data management plans (DMPs), database specifications, edit check specifications, data transfer agreements, and data review plans.
  • Actively participate in EDC system configuration and validation activities, including review of database builds, user acceptance testing (UAT), and system change control.
  • Perform ongoing hands-on data review, query trend analysis, and proactive data cleaning to ensure high-quality, analysis ready- datasets.

Technical Oversight & Data Quality
  • Partner with Clinical Operations and other groups to define and implement data quality standards, reconciliation strategies, and risk based-monitoring approaches for clinical data.
  • Lead hands-on-oversight of external CROs and vendors delivering data management services, including detailed review of deliverables, issue resolution, and escalation management.
  • Directly review and contribute to data listings, data exports, and interim analysis datasets in partnership with Biostatistics and Statistical Programming.
  • Ensure clinical trial data is compliant with applicable regulatory requirements, including GCP, ICH, and CDISC standards.
  • Support inspection readiness activities by authoring, reviewing, and maintaining data management documentation and responding directly to audit and inspection findings.

Cross Functional Collaboration
  • Partner closely with Clinical Operations to align data management activities with study execution, site operations, monitoring strategies, and operational reporting needs.
  • Collaborate with Biostatistics and Statistical Programming to ensure smooth handoff of clean, well documented- datasets for analysis and reporting.
  • Provide technical data management expertise to Regulatory Affairs in support of clinical study reports, INDs, BLAs, and other regulatory submissions.
  • Serve as the clinical data management subject matter- expert on study teams, governance forums, and internal reviews.

Process & Systems Ownership
  • Own and continuously improve clinical data management processes, tools, and SOPs to support efficient execution in a growing organization.
  • Evaluate, implement, and optimize clinical data systems and technologies (e.g., EDC, IRT, eCOA) to enhance data quality, traceability, and scalability.
  • Contribute hands-on to vendor selection, scope definition, and budgeting for data management services and systems.

The successful candidate will have:
  • Bachelor's degree or higher in life sciences, health informatics, computer science, or a related discipline with a minimum of 15 years of experience. Equivalent combinations of education and experience will be considered.
  • Significant experience in clinical data management within the biotechnology or pharmaceutical industry, including 8+ years of leadership of data management functions for clinical trials.
  • Demonstrated experience overseeing CROs and external vendors delivering clinical data management services.
  • Strong working knowledge of clinical trial processes, EDC systems, data standards, and regulatory expectations for clinical data.
  • Proven ability to lead teams, manage complex programs, and collaborate effectively in a fast-paced, matrixed environment.
  • Excellent written and verbal communication skills.

Preferred Qualifications:
  • Experience supporting oncology and/or cell or gene therapy clinical development programs.
  • Experience building or scaling clinical data management capabilities in a growing biotech organization.
  • Prior involvement in regulatory submissions and inspection readiness activities.

Physical Requirements
  • Preference to work onsite at least 2 days/week in our Seattle, WA or Louisville, CO location. If remote, the ability to travel to Seattle, WA at least once per quarter.
  • Ability to sit for prolonged periods of time.

Salary Range: $247,400 - $305,600
Benefits Offerings
Umoja Biopharma offers its employees competitive Medical, Dental, and Vision plans. Additionally, we offer Umojians access to a 401k plan through Fidelity, with a 100% match up to their first 4% deferral. Umoja also provides a generous Paid Time Off policy, employee commuter benefits, and cell phone stipend. For a full breakdown of our benefits offerings, please see the Benefits section of our website.

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