Clinical Research Assistant Jobs in Kansas
Clinical Research Assistant jobs in Kansas are concentrated in academic medical research, pharmaceutical testing, and hospital-based clinical trials, with demand at entry through mid-career levels across the state. Kansas City, Wichita, and Lawrence are the primary hiring hubs, where employers like the University of Kansas Health System, Stormont Vail Health, and the University of Kansas Medical Center consistently recruit for these roles. The most in-demand specialties are oncology trial coordination, cardiovascular research support, and regulatory data management. Scan the live roles below and apply to whichever ones fit.
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Showing 5 of 12+ Clinical Research Assistant jobs
Overland Park, United States of America | Full time | Field-based | R1577117
To be eligible for this position, you must reside in the same country where the job is located.
Essential Functions
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
- Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
- Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
- Collaborate and liaise with study team members for project execution support as appropriate.
- If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
- If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.
Qualifications
- Bachelor's Degree Degree in scientific discipline or health care preferred.
- Requires at least 3 years of year of on-site monitoring experience.
- Equivalent combination of education, training and experience may be accepted in lieu of degree.
- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.
- i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Good therapeutic and protocol knowledge as provided in company training.
- Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
- Written and verbal communication skills including good command of English language.
- Organizational and problem-solving skills.
- Effective time and financial management skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $74,500.00 - $197,500.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.Where you'll work
Field-based
You’ll work where the action is — out in the field, directly engaging with our customers, sites or partners. Field-based roles offer the opportunity to build relationships face-to-face, gain real-world insights and make a tangible impact.
Culture
Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.
Overland Park, United States of America | Full time | Field-based | R1577117
To be eligible for this position, you must reside in the same country where the job is located.
Essential Functions
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
- Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
- Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
- Collaborate and liaise with study team members for project execution support as appropriate.
- If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
- If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.
Qualifications
- Bachelor's Degree Degree in scientific discipline or health care preferred.
- Requires at least 3 years of year of on-site monitoring experience.
- Equivalent combination of education, training and experience may be accepted in lieu of degree.
- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.
- i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Good therapeutic and protocol knowledge as provided in company training.
- Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
- Written and verbal communication skills including good command of English language.
- Organizational and problem-solving skills.
- Effective time and financial management skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $74,500.00 - $197,500.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.Where you'll work
Field-based
You’ll work where the action is — out in the field, directly engaging with our customers, sites or partners. Field-based roles offer the opportunity to build relationships face-to-face, gain real-world insights and make a tangible impact.
Culture
Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.
See All 12 Clinical Research Assistant Jobs in Kansas
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Find JobsClinical Research Assistant Jobs by City in Kansas
Where Kansas roles are concentrated, by current openings.
Clinical Research Assistant Job Market in Kansas
A snapshot from current Kansas openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Biotechnology & Pharmaceuticals
- Consulting & Professional Services
What Kansas Employers Look For
The qualifications that appear most often in clinical research assistant jobs across Kansas.
- Bachelor's degree in life sciences, biology, or a health-related field required
- Familiarity with GCP guidelines and IRB submission processes strongly preferred
- Experience with electronic data capture systems such as REDCap or Medidata
- Strong attention to detail for accurate patient data collection and protocol compliance
- Ability to obtain CITI Program certification prior to or shortly after hire
- Prior clinical or research laboratory experience gained through internship or coursework
Clinical Research Assistant Jobs in Kansas: Frequently Asked Questions
How do you become a clinical research assistant in Kansas?
Most Kansas employers require a bachelor's degree in a life sciences field such as biology, biochemistry, or public health. Kansas does not issue a state license specifically for clinical research assistants, so the key credential is CITI Program certification in human subjects research, which many Kansas institutions require before study participation. Candidates who gain experience through the University of Kansas Medical Center's research programs or Stormont Vail Health's clinical departments are well positioned for entry-level roles.
Which companies hire clinical research assistants in Kansas?
Companies currently hiring clinical research assistants in Kansas include IQVIA, Altasciences, and Fortrea, per current listings on Migrate Mate as of November 2026. Academic health systems and hospital networks anchored in the Kansas City metro account for a significant share of ongoing openings in the state.
Which Kansas cities have the most clinical research assistant jobs?
Overland Park, Kansas, and Wichita have the most clinical research assistant openings in Kansas. The Kansas City metro dominates because of the University of Kansas Medical Center and its affiliated research institutes, while Wichita draws openings through Via Christi Health and Wesley Medical Center, and Lawrence benefits from proximity to University of Kansas research programs.
Are there remote clinical research assistant jobs in Kansas?
Yes, but they're rare. About 0% of clinical research assistant openings tied to Kansas are remote or hybrid as of November 2026, reflecting how hands-on the role typically is during active trial phases. The tasks most likely to be performed remotely are regulatory document preparation, data entry, and IRB correspondence rather than patient-facing study activities.
How can I get hired as a clinical research assistant in Kansas with little or no experience?
The most realistic entry path is applying as a research coordinator intern or study assistant at an academic medical center. The University of Kansas Medical Center and its affiliated Frontiers Clinical and Translational Science Institute regularly support students and new graduates in entry-level research roles. Transitioning from adjacent positions such as medical assistant, phlebotomist, or clinical data entry specialist is another common route. Completing CITI Program certification in advance and listing any coursework involving IRB protocols gives candidates a practical edge in Kansas applications.
Where can I find and apply to clinical research assistant jobs in Kansas?
You can find and apply to clinical research assistant jobs in Kansas on Migrate Mate, which lists current Kansas openings in one place. Search the listings for roles that match your experience and credentials, then apply directly to whichever ones fit your background.
See All 12 Clinical Research Assistant Jobs in Kansas
Find roles in Kansas that match your experience and apply in just a few clicks.
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