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  3. Senior Laboratory Coordinator - Cancer Center (Bioanalytical Lab)
UO

Senior Laboratory Coordinator - Cancer Center (Bioanalytical Lab)

University of Kansas Medical Center·Kansas City, Missouri

$28 - $38/hr·Full Time·On Site·2-5 yrs
·Posted 11 days ago
Practice for this role

About the role

Develop, validate, and apply UHPLC-MS/MS-based assays to quantify drugs and metabolites in clinical trial research samples. Maintain laboratory records, perform instrument calibrations, and collaborate with clinical research staff to ensure sample integrity and timely reporting.

Department

SOM KC Cancer Center Administration: -----

Clinical Research

Position title

Senior Laboratory Coordinator - Cancer Center (Bioanalytical Lab)

Job family group

Professional Staff

Job Description: SUMMARY:

The Senior Laboratory Coordinator will develop, validate, and apply UHPLC-MS/MS-based assays for quantitation of drugs, drug metabolites, and other small molecules in research samples collected from patients in clinical trials. In addition, maintain records for sample tracking in the lab and perform calibrations and minor maintenance on instruments and equipment.

The University of Kansas Cancer Center is the region's only National Cancer Institute-designated comprehensive cancer center where patients gain access to the most promising therapies, cutting-edge clinical trials and world class research.

Job description

Job Responsibilities

Develop, validate, and apply UHPLC-MS/MS-based assays for quantitation of drugs, drug metabolites, and other small molecules in research samples collected from patients in clinical trials.

Maintain records for sample tracking in the lab and perform calibrations and minor maintenance on instruments and equipment.

Utilize proven proficiency in basic laboratory skills — calibration and use of balances, pipettors, centrifuges, sample evaporators.

Perform, interpret, and report results from quantitative analytical methods.

Collaborate with Cancer Center laboratory and clinical research staff to ensure transfer and processing of samples and communication of results in a timely manner.

Ensure all requirements for sample integrity have been met (positive identification of patient, visit, and time; traceable records from sample transfer through final data delivery, etc.).

Recognize sources of error in sample identification, processing, or analysis and initiates corrective action when indicated. Assures the appropriate personnel have been contacted and the incident documented according to SOP’s.

Maintain records for sample tracking in the lab and performs calibrations and minor maintenance on instruments and equipment.

Participate in quality assurance/quality improvement activities related to sample transfer and storage, sample processing, sample analysis, and data integrity and reporting.

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 role will be 100% onsite.

Required Qualifications

Work Experience

  • Four (4) years of relevant work experience. Education may be substituted for experience on a year for year basis.
  • Experience with basic laboratory skills
  • calibration and use of balances, pipettors, centrifuges, sample evaporators.
  • Experience performing, interpreting, and reporting results from quantitative analytical methods.

Preferred Qualifications

Work Experience

  • Experience with mass spectrometry.
  • Experience with sample preparation techniques (protein precipitation, solid phase extraction, liquid-liquid extraction).
  • Experience with quantitative UHPLC-MS/MS procedures.
  • Experience in a regulated laboratory (GLP or equivalent).
  • Laboratory experience supporting clinical trials.

Skills

  • Interpersonal skills.
  • Time management.
  • Organization.
  • Attention to detail.
  • Multitasking.
  • Communication.
  • Critical thinking skills.
  • Computer skills.

Required Documents

  • Resume/CV
  • 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 [https://www.kumc.edu/human-resources/benefits.html]

Employee type

Regular

Time type: Full time

Rate type

Hourly

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

$28.20 - $38.35

Minimum

$28.20

Midpoint

$33.17

Maximum

$38.35

Requirements

Requires four years of relevant work experience or an equivalent combination of education and experience in basic laboratory skills and quantitative analytical methods. Preferred qualifications include experience with mass spectrometry, sample preparation techniques, and working in a GLP-regulated environment.

  • Interpersonal Skills
  • Multitasking
  • Communication
  • Time Management
  • Organization
  • Computer Skills
  • Attention to Detail
  • Critical Thinking
  • Sample Preparation
  • Clinical Trials
  • GLP
  • Mass Spectrometry
  • Quantitative Analytical Methods
  • UHPLC-MS/MS

Posting details

Employment type
Full Time
Work arrangement
On Site
Experience
2-5 yrs
Salary
$28 - $38/hr
Location
Kansas City, Missouri
Posted
Jul 17, 2026
Application
Employer website
UO

Hiring organization

University of Kansas Medical Center

The University of Kansas Health System in Kansas City is a world-class academic medical center and destination for complex care and diagnosis. We offer more options for patients with serious conditions because of our expertise and leadership in medical research and education....

Salary listed on 16 jobs
IndustryHospitals and Health Care
TypeNonprofit
Size10,001+ employees
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Market context

Missouri cancer lab coordination role

In Missouri, senior laboratory coordinator roles in cancer center and bioanalytical settings are often competitive because employers look for hands-on lab experience plus strong quantitative methods and regulated-environment familiarity. This position emphasizes four years of relevant experience, with preferred background in mass spectrometry, sample preparation, and GLP-regulated work. Review the AI-summarized requirements and benefits here to save time, then confirm your experience aligns with the lab techniques and compliance expectations before applying.

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