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Clinical Research Manager Jobs in Kansas (NOW HIRING)

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.

IQVIA

Clinical Research Coordinator

Wichita, KS · On-site

$35 - $42/hr

Clinical Research Coordinator - Wichita, KS Work Set-Up: On-site Schedule: Part-time, 24 hours per ... management while ensuring compliance with study protocols, regulatory requirements, and Good ...

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Clinical Research Manager information

See Kansas salary details

$43.7K

$95.7K

$168.6K

How much do clinical research manager jobs pay per year?

As of Sep 1, 2026, the average yearly pay for clinical research manager in Kansas is $95,728.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,200.00 and $109,300.00 per year, depending on experience, location, and employer.

What does a clinical research manager do?

A clinical research manager oversees clinical trials, which involve testing new medications or medical devices. Their responsibilities include ensuring all ethical practices and legal protocols are followed and that all paperwork is filled out completely and accurately. They also maintain standards for the data collection and procedures during the clinical trial and make sure all team members, including the doctors and nurses on the trial, are kept informed.

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

To thrive as a Clinical Research Manager, you need a solid understanding of clinical trial protocols, regulatory requirements (such as GCP), and a background in life sciences or healthcare, often supported by a relevant degree. Familiarity with clinical trial management systems (CTMS), EDC software, and certifications like ACRP or SOCRA are typically expected. Strong leadership, excellent organizational skills, and effective communication abilities set outstanding managers apart. These competencies are critical for ensuring compliance, data integrity, and the successful coordination of multidisciplinary research teams.

What are some common challenges clinical research managers face when overseeing multiple clinical trials simultaneously?

Clinical Research Managers often encounter challenges such as balancing competing timelines, ensuring regulatory compliance across different studies, and effectively allocating resources among projects. Managing communication between diverse teams—such as investigators, sponsors, and regulatory bodies—can also be demanding, especially when trials are at different stages. Developing strong organizational skills and leveraging project management tools are key to successfully navigating these complexities and maintaining high standards for data quality and participant safety.

What is the difference between Clinical Research Manager vs Clinical Research Coordinator?

AspectClinical Research ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with experience in project managementBachelor's in health sciences or related field, often with certification like CCRP
Work EnvironmentOversees multiple studies, manages teams, and ensures compliance at a higher levelAssists with daily study activities, patient interactions, and data collection
Employer & Industry UsagePharmaceutical companies, CROs, academic institutionsHospitals, clinics, research sites

The Clinical Research Manager focuses on overseeing entire studies and managing teams, while the Clinical Research Coordinator handles daily study tasks and participant interactions. Both roles require relevant certifications and are essential in clinical research settings, but they differ in scope and responsibilities.

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

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Clinical Research Manager jobs near you
Infographic showing various Clinical Research 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 $95,728 per year, or $46 per hour.

Clinical Research Coordinator

Tekton Research Inc

Wichita, KS • On-site

$21.50 - $28.75/hr

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Clinical Research Coordinator (CRC)

About Tekton Research:

Tekton Research is a growth-oriented clinical research organization committed to conducting high-quality clinical trials that advance medical knowledge and improve patient care. We are a collaborative, values-driven team that believes in Focus, Discipline, and Accountability. At Tekton Research, we take pride in doing excellent work while fulfilling our mission of Making Life Better.

We offer competitive compensation, comprehensive benefits, and opportunities for professional growth in a supportive and fast-paced research environment.

Position Summary:

The Clinical Research Coordinator (CRC) is responsible for the day-to-day coordination and management of clinical research studies, ensuring compliance with study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements. The CRC serves as the primary liaison between investigators, sponsors, study participants, and regulatory agencies while ensuring participant safety, data integrity, and successful study execution.

This role requires excellent organizational skills, strong attention to detail, and the ability to manage multiple clinical trials simultaneously in a dynamic environment.

Key Responsibilities: 

  • Coordinate and manage all aspects of assigned clinical trials from study start-up through close-out.
  • Recruit, screen, consent, and schedule study participants according to protocol requirements.
  • Collect, process, package, and ship laboratory specimens according to protocol and sponsor requirements.
  • Maintain accurate source documentation, regulatory binders, and study records in compliance with GCP, FDA regulations, and institutional policies.
  • Monitor participant safety and promptly identify, document, and report adverse events.
  • Prepare and submit regulatory documents, including Institutional Review Board (IRB) submissions, continuing reviews, and protocol amendments.
  • Collaborate with investigators, sponsors, monitors, and study staff to ensure successful study conduct.
  • Assist with monitoring visits, sponsor audits, and regulatory inspections.
  • Utilize Electronic Data Capture (EDC) systems and Clinical Trial Management Systems (CTMS) to maintain accurate study data.
  • Ensure protocol compliance while maintaining the highest standards of participant care and research integrity.

Required Qualifications:

  • High school diploma or GED required; Bachelor's degree in Nursing, Biology, Health Sciences, Public Health, or a related field preferred.
  • Minimum of one (1) year of Clinical Research Coordinator experience.
  • Working knowledge of Good Clinical Practice (GCP), FDA regulations, ICH guidelines, and clinical research processes.
  • Experience with pediatric and adult phlebotomy and specimen processing.
  • Strong organizational and time management skills with the ability to prioritize multiple studies.
  • Experience maintaining regulatory documentation and source records.
  • Proficiency with Electronic Data Capture (EDC) systems and Microsoft Office applications.
  • Excellent verbal and written communication skills.
  • Ability to work independently while collaborating effectively with multidisciplinary teams.

Preferred Qualifications:

  • Current ACRP-CRC or SOCRA certification.
  • Advanced degree in Nursing, Public Health, Clinical Research, or a related healthcare field.
  • Experience working on industry-sponsored or multi-center clinical trials.
  • Familiarity with clinical monitoring, participant recruitment, and retention strategies.

Why Join Tekton Research?

At Tekton Research, you'll join a team dedicated to excellence, innovation, and improving lives through clinical research. We foster a collaborative culture where professional development is encouraged, contributions are valued, and every team member plays an important role in advancing healthcare.

If you are passionate about clinical research and committed to providing exceptional patient care, we encourage you to apply and become part of the Tekton Research team.

Apply