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Commission Cancer Data Management Jobs in Kansas

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Commission Cancer Data Management information

What is Commission Cancer Data Management?

Commission Cancer Data Management refers to the specialized process of collecting, managing, and analyzing cancer patient data as required by the Commission on Cancer (CoC), a program of the American College of Surgeons. Professionals in this field ensure accurate, complete, and timely reporting of cancer cases for hospitals and cancer registries. Their work supports accreditation standards, helps improve patient care, and contributes to cancer research by maintaining high-quality data. They typically use specialized software and follow strict guidelines to ensure data integrity and compliance with regulatory requirements.

What are the key skills and qualifications needed to thrive as a Commission Cancer Data Manager?

To thrive as a Commission Cancer Data Manager, you need a strong background in medical records management, cancer registry operations, and knowledge of oncology, often supported by a Certified Tumor Registrar (CTR) credential. Familiarity with cancer registry software, electronic health records (EHRs), and data coding systems such as ICD-O is typically required. Attention to detail, analytical thinking, and effective communication are essential soft skills for ensuring data accuracy and collaborating with healthcare teams. These skills and qualifications are vital for maintaining high-quality cancer data, supporting accreditation, and informing patient care and research.

What are some common challenges faced by professionals in Commission Cancer Data Management, and how can they be addressed?

Professionals in Commission Cancer Data Management often encounter challenges such as ensuring data accuracy, keeping up with evolving reporting standards, and managing large volumes of complex patient information. Addressing these challenges typically involves ongoing training on data abstraction and registry software, regular collaboration with clinical teams to clarify ambiguous cases, and proactive review of Commission on Cancer (CoC) updates. Staying connected with professional organizations and participating in peer networking can also help share best practices and solutions to common obstacles.
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Infographic showing various Commission Cancer Data Management job openings in Kansas as of June 2026, with employment types broken down into 91% Full Time, 5% Part Time, and 4% Contract. Highlights an 74% In-person, and 26% Remote job distribution.

Clinical Research Coordinator - Cancer Center

KUMC University of Kansas Medical Center

Kansas City, KS

$23.50 - $31/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 2 days ago

Job description

Department:SOM KC Cancer Center Clinical Trials

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Clinical ResearchPosition Title:Clinical Research Coordinator - Cancer CenterJob Family Group: Professional StaffJob Description Summary:The Clinical Research Coordinator works collaboratively with multidisciplinary teams, research, and hospital staff to recruit, screen, educate, and assist in the overall clinical study coordination of clinical research. This position manages assigned clinical research studies by supervising a variety of complex activities involved in the collection, compilation, documentation, and analysis of clinical research data. Monitors participants' progress including documenting and reporting adverse events. Participates in periodic quality assurance audits of protocols.
The University of Kansas Cancer Center is the only National Cancer Institute designated Comprehensive Cancer Center in the region, 1 of only 57 in the nation to receive this distinction. Patients gain access to the most promising therapies, cutting-edge clinical trials and world class research.Job Description:

Job Responsibilities

  • Under the direction of the principal investigator, recruit and educate potential patients for and evaluate potential patient eligibility for clinical trials.

  • Maintain source documents and submit case report forms (CRFs) as required for clinical trials.

  • Recognize and report adverse events/serious adverse events to the Principal Investigator, FDA, and sponsors.

  • Perform study procedures, as outlined in the protocol and within state and institutional scope of practice.

  • Assist clinical staff with phlebotomy and sample collection, processing, handling, and shipping as outlined in the protocol and within institutional/KUMC policy.

  • Ensure adequate study supplies are being maintained. Track study expenditures and submit reimbursement requests for study equipment, supplies and study participants.

  • Prepare documentation and participate in study monitoring visits, reviews and audits. Provide written and verbal reports to Principal Investigator and Project Manager, as required.

  • Participate in quality assurance activities by reviewing clinical data in medical record charts, assessing pharmacy compliance with protocol criteria and reviewing study documentation to ensure compliance with GCP guidelines and FDA CFR.

  • Work closely with the Research Institute and Human Research Protection Program and have a working knowledge of KUMC policies and procedures.

  • Attend continuing education, research and training seminars as requested by manager.

This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. It is only a summary of the typical functions of the job, not an exhaustive list of all possible job responsibilities, tasks, duties, and assignments. Furthermore, job duties, responsibilities and activities may change at any time with or without notice.

Work Environment: This position will be 100% onsite due to the fact this is a patient facing role.

Required Qualifications

Work Experience:

  • 4 years of relevant work experience. Education may be substituted for experience on a year for year basis.

  • Experience with regulations governing clinical research (CFR, GCP, HIPAA).

  • Experience with statutes and guidelines relevant to regulatory affairs in clinical research.

  • Experience using MS Office products.

Preferred Qualifications

Education: Bachelor's degree.

Work Experience:

  • Experience study budgets, contracts, and grant applications.

Certifications/Licenses:

  • Certified Clinical Research Coordinator (CCRC)

  • Certified Clinical Research Professional (CCRP)

Skills

  • Attention to detail

  • Time Management

  • Interpersonal Skills

  • Communication.

  • Organization.

  • Multi-tasking.

Required Documents

  • Resume

  • Cover Letter

Comprehensive Benefits Package:

Coverage begins on day one for health, dental, and vision insurance and includes health expense accounts with generous employer contributions if the employee participates in a qualifying health plan. Employer-paid life insurance, long-term disability insurance, and various additional voluntary insurance plans are available. Paid time off, including vacation and sick, begins accruing upon hire, plus ten paid holidays. One paid discretionary day is available after six months of employment, and paid time off for bereavement, jury duty, military service, and parental leave is available after 12 months of employment. A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. https://www.kumc.edu/human-resources/benefits.html

Employee Type: RegularTime Type: Full timeRate Type: Salary

Compensation Statement:

The pay range listed for this position is determined by our compensation program using market data and salary benchmarking. A combination of factors is considered in making compensation decisions including, but not limited to, education, experience and training, qualifications relative to the requirements of the position, and funding. At the University of Kansas Medical Center, a reasonable estimate for the starting pay range will be the minimum to midpoint of the posted range, taking into account the combination of factors listed above.

Pay Range:$60,800.00 - $91,200.00

Minimum

$60,800.00

Midpoint

$76,000.00

Maximum

$91,200.00

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