Clinical Research Jobs in Kansas
Clinical Research jobs in Kansas are concentrated in Wichita, Kansas City, and Lawrence, where research-active institutions and life sciences employers maintain steady hiring at the coordinator, associate, and principal investigator levels. Major employers with a lasting footprint in the state include the University of Kansas Health System, Wichita's Wesley Medical Center, and Labcorp Drug Development, which runs clinical operations across the region. Demand is most consistent for professionals with experience in oncology trials, cardiovascular studies, and regulatory affairs. Scan the live roles below and apply to whichever ones fit.
Find Clinical Research JobsOverview
Showing 5 of 10+ Clinical Research jobs
Your New Company!
At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences.
We are better together and together We Are Altasciences.
About The Role
The Clinical Research Nurse II will oversee the safety and consent of clinical trial participants during study conduct and the maintenance of safety equipment. The Clinical Research Nurse II will execute tasks performed in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs).
Work Schedule: Evenings/Overnight
What You'll Do Here
- Perform scheduled inspection of emergency crash carts, inventory/inspect the contents, and maintain up to date records.
- May train employees on clinical trial activities associated to their job’s needs.
- Ensure the confidentiality of clinical trial participants and sponsors is respected.
- Perform clinical trial activities including but not limited to, continuous safety monitoring, safety assessments, Investigational Product (IP) administration and catheter installation.
- Monitor, document and/or follow-up on participant adverse events.
- Maintain and advocate a high level of patient care, quality, and safety within the department.
- May assist in study related consenting with participant screenings.
- Provide feedback, where necessary, to appropriate team members of study progress.
- Proactively communicate issues and/or problem resolutions to departmental supervisors and managers.
- Other tasks as assigned by management
What You'll Need to Succeed
Education:
Degree from accredited Registered Nurse program required or bachelor’s degree in nursing from an accredited school.
Work Experience:
Minimum of 4+ years of related clinical research experience required.
Certificates/Licenses /Registrations:
US requirements:
- Current Registered Nurse (RN) license, required
- Current Basic Life Support (BLS, CPR/AED) certification, required
- Current Advanced Cardiac Life Support (ACLS) certification, required
Canadian requirements:
- Ordre des infirmières et infirmiers du Québec (OIIQ) permit
- Cardiopulmonary resuscitation (CPR) certification, required.
Advanced Cardiovascular Life Support (ACLS) certifications, required
Technical Skills:
Microsoft suite
Strong computer literacy
Language(s) Skills:
- Ability to read and interpret technical documents and industry specific manuals.
- Ability to write advanced reports and correspondence.
- Ability to speak effectively before groups of customers or employees of the organization.
- Bilingual proficiency in French may be required, depending on location.
Other Requirements:
- Excellent verbal and written communication skills.
- Well-developed interpersonal skills are required.
- Personal/professional integrity and proven discretion in handling confidential information.
- Capable of managing multiple conflicting priorities.
- Relevant industry experience a plus.
MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH
Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences!
Your New Company!
At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences.
We are better together and together We Are Altasciences.
About The Role
The Clinical Research Nurse II will oversee the safety and consent of clinical trial participants during study conduct and the maintenance of safety equipment. The Clinical Research Nurse II will execute tasks performed in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs).
Work Schedule: Evenings/Overnight
What You'll Do Here
- Perform scheduled inspection of emergency crash carts, inventory/inspect the contents, and maintain up to date records.
- May train employees on clinical trial activities associated to their job’s needs.
- Ensure the confidentiality of clinical trial participants and sponsors is respected.
- Perform clinical trial activities including but not limited to, continuous safety monitoring, safety assessments, Investigational Product (IP) administration and catheter installation.
- Monitor, document and/or follow-up on participant adverse events.
- Maintain and advocate a high level of patient care, quality, and safety within the department.
- May assist in study related consenting with participant screenings.
- Provide feedback, where necessary, to appropriate team members of study progress.
- Proactively communicate issues and/or problem resolutions to departmental supervisors and managers.
- Other tasks as assigned by management
What You'll Need to Succeed
Education:
Degree from accredited Registered Nurse program required or bachelor’s degree in nursing from an accredited school.
Work Experience:
Minimum of 4+ years of related clinical research experience required.
Certificates/Licenses /Registrations:
US requirements:
- Current Registered Nurse (RN) license, required
- Current Basic Life Support (BLS, CPR/AED) certification, required
- Current Advanced Cardiac Life Support (ACLS) certification, required
Canadian requirements:
- Ordre des infirmières et infirmiers du Québec (OIIQ) permit
- Cardiopulmonary resuscitation (CPR) certification, required.
Advanced Cardiovascular Life Support (ACLS) certifications, required
Technical Skills:
Microsoft suite
Strong computer literacy
Language(s) Skills:
- Ability to read and interpret technical documents and industry specific manuals.
- Ability to write advanced reports and correspondence.
- Ability to speak effectively before groups of customers or employees of the organization.
- Bilingual proficiency in French may be required, depending on location.
Other Requirements:
- Excellent verbal and written communication skills.
- Well-developed interpersonal skills are required.
- Personal/professional integrity and proven discretion in handling confidential information.
- Capable of managing multiple conflicting priorities.
- Relevant industry experience a plus.
MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH
Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences!
See All 10 Clinical Research Jobs in Kansas
Find roles in Kansas that match your experience and apply in just a few clicks.
Find Clinical Research JobsClinical Research Jobs by City in Kansas
Where Kansas roles are concentrated, by current openings.
Clinical Research Job Market in Kansas
A snapshot from current Kansas openings, updated as new roles post.
Who's Hiring
What Kansas Employers Look For
The qualifications that appear most often in clinical research jobs across Kansas.
- Bachelor's degree in life sciences, nursing, or a health-related field required
- CCRP or CCRC certification from ACRP or SOCRA preferred or required
- Experience managing clinical trial protocols under ICH-GCP guidelines
- Proficiency with electronic data capture systems such as REDCap or Medidata Rave
- Strong regulatory document management and IRB submission experience
- Ability to coordinate multi-site studies and communicate with sponsor representatives
Clinical Research Jobs in Kansas: Frequently Asked Questions
How do you become a clinical research in Kansas?
The most direct path is earning a bachelor's degree in a life sciences, nursing, or health-related field and then completing the Certified Clinical Research Coordinator credential offered through the Association of Clinical Research Professionals or the Society of Clinical Research Associates. Kansas does not require a separate state license specific to clinical research coordinators, so hiring decisions hinge primarily on GCP training, hands-on trial experience, and certification status recognized by major Kansas employers such as the University of Kansas Health System.
Which companies hire clinical researchs in Kansas?
Kansas clinical research roles are posted by IQVIA, Altasciences, and Kansas City Card Arrhythmia Research and others right now, based on current listings on Migrate Mate as of August 2026. The University of Kansas Health System and its affiliated research centers are among the most consistent sources of openings, particularly for coordinator and regulatory roles tied to federally funded studies.
Which Kansas cities have the most clinical research jobs?
Overland Park, Topeka, and Kansas City account for the largest share of clinical research openings in Kansas. Wichita leads because of its concentration of hospital systems and Labcorp Drug Development operations, Kansas City draws from the University of Kansas Health System and its research campus, and Lawrence benefits from its proximity to the University of Kansas main campus and affiliated clinical programs.
Are there remote clinical research jobs in Kansas?
Yes, but they're less common than in purely desk-based fields because many clinical research roles require on-site patient contact, specimen handling, or direct study monitoring. About 0% of clinical research openings tied to Kansas are remote or hybrid as of August 2026, reflecting the share of positions focused on data management, regulatory affairs, and remote site monitoring rather than hands-on trial coordination.
How can I get hired as a clinical research in Kansas with little or no experience?
The most realistic entry path is applying as a clinical research assistant or study coordinator assistant at one of Kansas's large academic medical centers, particularly the University of Kansas Health System, which periodically posts entry-level research support roles open to recent graduates. Candidates with a background in medical assisting, pharmacy technician work, or clinical data entry have a natural advantage because those roles share overlapping skills. Completing a GCP training course and earning a CCRP credential, even before your first trial job, signals readiness to Kansas hiring managers and separates applicants with no trial experience from the rest.
Where can I find and apply to clinical research jobs in Kansas?
You can find and apply to clinical research jobs in Kansas on Migrate Mate, which lists current Kansas openings across Wichita, Kansas City, Lawrence, and other markets in the state. Search the listings, find the roles that match your experience and credentials, and apply directly to the ones that fit.
See All 10 Clinical Research Jobs in Kansas
Find roles in Kansas that match your experience and apply in just a few clicks.
Find Clinical Research Jobs