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Clinical Study Manager Jobs in Kansas (NOW HIRING)

micro1 AI

Medical Writing Manager

Overland Park, KS · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...

micro1 AI

Medical Writing Manager

Kansas City, KS · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...

micro1 AI

Medical Writing Manager

Olathe, KS · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...

micro1 AI

Medical Writing Manager

Wichita, KS · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...

micro1 AI

Medical Writing Manager

Topeka, KS · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...

EmVenio Research

Clinical Research Coordinator

Kansas City, KS · On-site

$23.25 - $31/hr

You work with a high attention to detail, reviewing documentation, coordinating clinical study ... Consults with the Site Manager and virtual Clinical Research Coordinator to ensure compliance with ...

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All JobsClinical Study JobsClinical Study Manager JobsClinical Study Manager Jobs in Kansas

Clinical Study Manager information

See Kansas salary details

$25

$55

$85

How much do clinical study manager jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for clinical study manager in Kansas is $55.76, according to ZipRecruiter salary data. Most workers in this role earn between $45.24 and $62.84 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical study manager?

To thrive as a Clinical Study Manager, you need a strong background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications like GCP (Good Clinical Practice) are highly valued. Strong organizational, leadership, and communication skills help manage cross-functional teams and ensure study timelines are met. These skills are crucial for maintaining study quality, ensuring regulatory adherence, and delivering successful trial outcomes.

What are some common challenges faced by clinical study managers, and how can they be addressed?

Clinical Study Managers often encounter challenges such as coordinating multiple stakeholders, ensuring regulatory compliance, and managing tight timelines across study sites. Effective communication and proactive planning are essential to address these issues, as well as staying up to date with changing industry regulations. Building strong relationships with site staff and fostering a collaborative team environment can also help mitigate delays and ensure study milestones are met successfully.

How much does a clinical study manager earn?

A clinical study manager's salary varies based on experience, location, and the size of the organization, but typically ranges from $80,000 to $130,000 annually. Senior roles or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. The position often requires knowledge of regulatory guidelines and project management tools.

What does a clinical study manager do?

A clinical study manager oversees the planning, execution, and monitoring of clinical trials to ensure they comply with regulatory standards and protocols. They coordinate with research teams, manage timelines and budgets, and ensure data quality, often using specialized software and requiring knowledge of Good Clinical Practice (GCP) guidelines.

What are the most commonly searched types of Clinical Study jobs in Kansas?

The most popular types of Clinical Study jobs in Kansas are:

What are popular job titles related to Clinical Study Manager jobs in Kansas?

For Clinical Study Manager jobs in Kansas, the most frequently searched job titles are:

What job categories do people searching Clinical Study Manager jobs in Kansas look for?

The top searched job categories for Clinical Study Manager jobs in Kansas are:

What cities in Kansas are hiring for Clinical Study Manager jobs?

Cities in Kansas with the most Clinical Study Manager job openings:

Clinical Study Manager jobs near you
Infographic showing various Clinical Study Manager job openings in Kansas as of August 2026, with employment types broken down into 86% Full Time, 12% Part Time, 1% Temporary, and 1% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $115,971 per year, or $55.8 per hour.

Clinical Research Coordinator - Cancer Center

Kansas City, KS

KUMC University of Kansas Medical Center
See more jobs at KUMC University of Kansas Medical Centerexternal

$23.50 - $31/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 7 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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