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Clinical Research Operations Manager Jobs in Kansas

Tekton Research Inc

Clinical Research Coordinator

Wichita, KS · On-site

$21.50 - $28.75/hr

Clinical Research Coordinator (CRC) About Tekton Research: Tekton Research is a growth-oriented ... Coordinate and manage all aspects of assigned clinical trials from study start-up through close-out.

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Grene Vision Group

Clinical Research Coordinator

Wichita, KS · On-site

$21.75 - $28.75/hr

Employee Discounts JOB SUMMARY The Clinical Research Coordinator provides clinical research support for studies involving human subjects and manages the daily operations of clinical trials. Duties ...

IQVIA

Manager, Clinical Operations

Overland Park, KS

$86K - $216K/yr

Participate in the allocation of resources to clinical research projects by assigning staff to ... clinical operations management. May collaborate with other clinical teams and other functional ...

IQVIA, Inc.

Manager, Clinical Operations

Overland Park, KS · On-site

$86K - $216K/yr

... operations management. • May collaborate with other clinical teams and other functional ... IQVIA is a leading global provider of clinical research services, commercial insights and health ...

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All JobsClinical Research Operations JobsClinical Research Operations Manager JobsClinical Research Operations Manager Jobs in Kansas

Clinical Research Operations Manager information

See Kansas salary details

$31.2K

$87.4K

$166.3K

How much do clinical research operations manager jobs pay per year?

As of Aug 4, 2026, the average yearly pay for clinical research operations manager in Kansas is $87,436.00, according to ZipRecruiter salary data. Most workers in this role earn between $64,700.00 and $101,200.00 per year, depending on experience, location, and employer.

How does a clinical research operations manager collaborate with cross-functional teams during a study?

As a Clinical Research Operations Manager, you will work closely with cross-functional teams including clinical trial coordinators, data managers, regulatory affairs specialists, and principal investigators. Your role involves facilitating clear communication between departments, ensuring that study milestones are met, and resolving operational issues as they arise. Regular meetings and status updates are common, and you'll often act as a liaison to keep all stakeholders aligned on study objectives, timelines, and compliance requirements. This collaborative approach is crucial for maintaining study integrity and ensuring successful trial outcomes.

What does a clinical research operations manager do?

A Clinical Research Operations Manager oversees the daily operations of clinical trials to ensure they are conducted efficiently, ethically, and in compliance with regulatory standards. They coordinate between research staff, sponsors, and regulatory bodies, manage budgets and timelines, and ensure proper documentation and reporting. Their role is essential in maintaining the quality and integrity of clinical studies from start to finish.

What are the key skills and qualifications needed to thrive as a clinical research operations manager, and why are they important?

To thrive as a Clinical Research Operations Manager, you need a solid background in clinical research, regulatory compliance, and project management, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and certifications such as ACRP or SOCRA are highly valuable. Leadership, problem-solving, and excellent organizational and communication skills help you manage teams and collaborate effectively with stakeholders. These skills and qualities are crucial for ensuring the successful execution of clinical trials while maintaining regulatory standards and operational efficiency.
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Clinical Research Operations Manager jobs near you
Infographic showing various Clinical Research Operations Manager job openings in Kansas as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $87,436 per year, or $42 per hour.

Senior Regulatory Coordinator - Comprehensive Integrated Research Operations (CIRO)

KUMC University of Kansas Medical Center

Kansas City, KS

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 13 days ago

Job description

Department:Comprehensive Integrated Research Operations (CIRO)

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AdministrationPosition Title:Senior Regulatory Coordinator - Comprehensive Integrated Research Operations (CIRO)Job Family Group: Professional StaffJob Description Summary:The Senior Regulatory Coordinator within the Comprehensive Integrated Research Operations (CIRO) department serves as the administrative resource and liaison involved in supporting the business aspects of the clinical research enterprise. The Senior Regulatory Coordinator is responsible for leading and performing study-specific regulatory and safety reporting for a group of investigators, within multiple cost centers in the Department of Internal Medicine. This position is responsible for ensuring that the research is compliant with applicable federal, state, or international requirements, while adhering to policies of the University of Kansas Medical Center. This individual will support study-start up activities including IRB/Ancillary committee submissions, and maintenance of regulatory records throughout the life project for assigned cost centers.Job Description:

Job Duties:

  • Assist PI with investigator-initiated studies across multiple agencies, including protocol development, reviewing consent forms, budget planning and following-up with system set-up.
  • Interface with study sponsors and study team members during study start-up and maintenance regarding regulatory documents, other regulatory issues, or contract modifications.
  • Provide updates as required, escalate as appropriate.
  • Lead Internal Medicine's Quality Improvement activities for Clinical Research Enterprise.
  • Perform study start-up activities, including submission of study documents to the Institutional Review Board (IRB).
  • Maintain study timeline goals, monitor progress, and escalate delays appropriately.
  • Collaborate with study team members to ensure regulatory documents are completed accurately and in accordance with requirements.
  • Complete and maintain study file documents according to the requirements of ICH GCP E6 and applicable Regulatory Agency guidance and standards.
  • Update protocol and study information into the Clinical Trial Management System (Velos) for team collaboration.
  • Provide assistance to study monitors during routine monitor visits or audits.
  • Support internal implementation of general principles of GAAP standards in reviewing financial compliance and consistency with contracts/agreements over the life of the project, following institutional and sponsor guidelines.
  • Support the management or perform analytical and financial activities associated with cost studies, forecasting, planning, and managing clinical portfolios, including close-out of projects.
  • Facilitate reporting and updates to study teams on the financial status of the clinical projects.
  • Manage and perform activities related to multiple areas of clinical research project administration, including cross-functional duties and responsibilities across clinical research projects.

This job description is not designed to 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, duties, and assignments. Furthermore, job duties and responsibilities may change at any time with or without notice.

Required Qualifications

Work Experience:

  • Six (6) years of work experience in healthcare or research setting. Relevant education may be substituted for experience on a year for year basis.
  • Experience in a environment requiring an understanding of regulations governing clinical research (CFR, GCP, HIPAA) and statutes and guidelines relevant to regulatory affairs in clinical research.

Required Certifications:Research certification such as:

  • Certified Clinical Research Coordinator (CCRC).
  • Certified Clinical Research Professional (CCRP).
  • Association of Clinical Research Professionals (ACRP).

Preferred Qualifications

Education:

  • Master's Degree in health sciences, biology, nursing, or a related field.

Work Experience:

  • Two (2) years of work experience in healthcare or research setting.

Skills

  • Communication
  • Multitasking
  • Time management
  • Interpersonal skills
  • Computer skills

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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