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Protocol Coordinator Jobs in Kansas (NOW HIRING)

Studio Coordinator-Newton

Newton, KS · On-site

$11.50 - $15/hr

ROLE SUMMARY As a Studio Coordinator (SC), you live your power by supporting the world class ... Support communication around Smart Health Protocol to students upon entry and throughout their ...

Clinical Research Coordinator

Wichita, KS · On-site

$21.75 - $28.75/hr

Clinical Research Coordinator DEPARTMENT: Clinical Research LOCATION: Wichita, KS PERKS * Full ... Evaluate protocols, assist in study selection, correspond/coordinate with the sponsor/CRO and ...

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Showing results 1-20

Protocol Coordinator information

See Kansas salary details

$24.1K

$51.6K

$90.5K

How much do protocol coordinator jobs pay per year?

As of Aug 27, 2026, the average yearly pay for protocol coordinator in Kansas is $51,610.00, according to ZipRecruiter salary data. Most workers in this role earn between $36,100.00 and $62,000.00 per year, depending on experience, location, and employer.

What is a protocol coordinator?

Protocol coordinators are professionals responsible for managing and overseeing the implementation of clinical trial protocols or research studies. They ensure that all activities are conducted in compliance with regulatory requirements, ethical standards, and the specific guidelines of the study protocol. Their duties often include organizing study logistics, coordinating communications between investigators and sponsors, maintaining accurate documentation, and ensuring participant safety. Protocol coordinators play a crucial role in ensuring the smooth and efficient operation of clinical research projects.

What are the key skills and qualifications needed to thrive as a protocol coordinator, and why are they important?

To thrive as a Protocol Coordinator, you need strong organizational skills, attention to detail, and a background in clinical research or project management, often supported by a relevant bachelor's degree. Familiarity with regulatory compliance systems, clinical trial management software (CTMS), and protocols such as Good Clinical Practice (GCP) is typically required. Excellent communication, problem-solving, and multitasking abilities help you effectively coordinate between stakeholders and manage complex timelines. These skills ensure the smooth execution of protocols, regulatory compliance, and the successful progression of clinical studies or organizational processes.

What are some common challenges protocol coordinators face when managing complex meetings or events?

Protocol Coordinators often encounter challenges such as balancing the needs and expectations of diverse stakeholders, ensuring strict adherence to diplomatic protocols, and managing last-minute changes in schedules or guest lists. Successfully navigating cultural sensitivities and maintaining effective communication with both internal teams and external partners are key to overcoming these obstacles. Flexibility, attention to detail, and strong organizational skills are essential for addressing unexpected issues while maintaining a professional environment.

What is the difference between Protocol Coordinator vs Clinical Research Associate?

AspectProtocol CoordinatorClinical Research Associate
Required CredentialsTypically a bachelor's degree in health sciences, life sciences, or related field; certifications like CCRP are a plusUsually a bachelor's degree in life sciences or health sciences; certifications like CCRP or CRA are common
Work EnvironmentOffice-based, coordinating clinical trial protocols, communicating with sites and teamsMonitoring clinical sites, ensuring compliance, and data accuracy during trials
Employer & Industry UsagePharmaceutical companies, research institutions, CROsPharmaceutical companies, CROs, research organizations

While both roles support clinical trials, Protocol Coordinators focus on managing trial protocols and communication, whereas Clinical Research Associates primarily monitor trial sites and ensure compliance. Both roles require similar educational backgrounds and certifications, often working within the same industry environments.

How long does it take to become a protocol coordinator?

Becoming a protocol coordinator typically requires a bachelor's degree in a related field such as healthcare, life sciences, or research, which takes about four years. Gaining relevant experience in clinical research or project management can take an additional 1-3 years, depending on the individual's background and the complexity of the role.

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

The most popular types of Protocol jobs in Kansas are:

What are popular job titles related to Protocol Coordinator jobs in Kansas?

For Protocol Coordinator jobs in Kansas, the most frequently searched job titles are:

What cities in Kansas are hiring for Protocol Coordinator jobs?

Cities in Kansas with the most Protocol Coordinator job openings:

Infographic showing various Protocol Coordinator job openings in Kansas as of August 2026, with employment types broken down into 88% Full Time, and 12% Part Time. Highlights an 100% In-person job distribution, with an average salary of $51,610 per year, or $24.8 per hour.

Full-time

Posted 7 days ago


University Of Kansas Health System rating

7.5

Company rating: 7.5 out of 10

Based on 179 frontline employees who took The Breakroom Quiz

236th of 894 rated healthcare providers


Job description

Position Title
Policy CoordinatorDays - Full TimeDelp PavilionPosition Summary / Career Interest:The Policy Coordinator is responsible for managing and maintaining the policies and protocols of individual University of Kansas Health System locations. This includes overseeing the development, coordination, management, publishing and archiving of policies and protocols. The Policy Coordinator will work closely with leaders throughout the organization to maintain their policies and protocols. The Policy Coordinator oversees the day-to-day management of the health system's online policy management system and may serve as a site administrator for one or more health system locations. The Policy Coordinator may also serve as a back-up to the Health System Policy Administrator and is a member of the Accreditation/Regulatory Compliance department.Responsibilities and Essential Job Functions
  • Responsible for maintaining the policy management system for individual health system locations, serving as a site administrator.
  • Assist the Health System Policy Administrator with onboarding of newly acquired hospitals to the health system and providing orientation and training to site administrators and document owners/ approvers.
  • Perform routine tasks in the policy management system, such as building approval workflows and standardizing policy areas with health system standards.
  • Review documents prior to final posting to ensure documents represent the health system and hospital's mission and vision, meet federal and state regulations, accreditation standards and evidence-based guidelines.
  • Communicate policy and protocol documents in an organized format with version controls and tracking of changes in an organized format, assuring an archival tracking of all versions.
  • Maintain and coordinate the system's policies and protocols to ensure they are evidence-based and current in system's online policy management system.
  • Assures all new and revised documents include an education plan appropriate to the process involved, as applicable.
  • Coordinate the process of preparing documents for review and approval through applicable committees.
  • Able to develop documents that are concise, correct and clearly understandable, with correct grammar and formatting.
  • Participate (and may lead) in policy and protocol related projects as assigned.
  • Organize policy and procedure meetings, take minutes, and communicate pre-meeting and follow-up information to committee members.
  • Work closely with and serve as a resource to document owners/ approvers at health system hospitals.
  • Serve as a resource for staff, physicians and leadership regarding policies and protocols.
  • Monitor documents for compliance with required review dates.
  • Participate in system tracers and regulatory surveys as assigned.
  • Must be self-motivated, highly organized and able to keep track of many processes and documents at the same time.
  • Correctly use and spell medical terms.
  • Able to skillfully communicate and partner with others via email, telephone and in person.
  • Able to teach, share information and develop presentations.
  • Use time efficiently and effectively. Able to develop and meet project time frames.
  • Must be able to perform the professional, clinical and or technical competencies of the assigned unit or department.
  • These statements are intended to describe the essential functions of the job and are not intended to be an exhaustive list of all responsibilities. Skills and duties may vary dependent upon your department or unit. Other duties may be assigned as required.

Required Education and Experience
  • High School Graduate
  • 3 or more years experience in organizing and maintaining documents using an online system.

Preferred Education and Experience
  • Bachelors Degree from an accredited College or University.
  • 1 or more years experience with medical terminology.

Required Language Skills
  • Advanced English - read, write and speak English

Knowledge Requirements
  • Excellent communication, writing, organizational and presentation skills; demonstrates superior oral and written communication and time management skills.
  • Understanding of medical terminology.
  • Advanced working knowledge of Microsoft Office, including Word and Excel.
  • Travel to off-site health system locations throughout the state of Kansas and Missouri.
Time Type:Full timeJob Requisition ID:R-56253Important information for you to know as you apply:
  • The health system is an equal employment opportunity employer. Qualified applicants are considered for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, ancestry, age, disability, veteran status, genetic information, or any other legally-protected status. See also Diversity, Equity & Inclusion.

  • The health system provides reasonable accommodations to qualified individuals with disabilities. If you need to request reasonable accommodations for your disability as you navigate the recruitment process, please let our recruiters know by requesting an Accommodation Request form using this link asktalentacquisition@kumc.edu.

  • Employment with the health system is contingent upon, among other things, agreeing to the health-system-dispute-resolution-program.pdf and signing the agreement to the DRP.

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About University of Kansas Health System

Sourced by ZipRecruiter

Operating within the healthcare industry, The University of Kansas Health System is a renowned medical institution located in Kansas City, KS, United States. Established in 1905, this not-for-profit health system has evolved to offer an extensive range of products and services, which spans across a variety of specialist areas such as cancer care, neurology, cardiology, and organ transplants, among others. The core mission of The University of Kansas Health System is to enhance the health and wellness of individuals and communities by providing world-class healthcare services, quality education and conducting advanced research. They are also known for their unwavering commitment to academic medicine, which sets them apart from their peers.

Industry

Health care and social assistance

Company size

5,001 - 10,000 Employees

Headquarters location

Kansas City, KS, US