Clinical Research Manager Jobs in Kansas
Clinical Research Manager jobs in Kansas are consistently active, concentrated in pharmaceutical research, academic medical centers, and regional hospital networks, with openings at both mid-level coordinator-to-manager transitions and senior oversight roles. Wichita, Kansas City, and Lawrence anchor most of the hiring, where established employers like the University of Kansas Health System, Pfizer's Kansas operations, and Cerner (now Oracle Health) maintain ongoing clinical research programs. The most in-demand specialties are oncology trial management, regulatory compliance oversight, and multi-site study coordination. Scan the live roles below and apply to whichever ones fit.
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Showing 5 of 10+ Clinical Research Manager 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 Manager Jobs in Kansas
Find roles in Kansas that match your experience and apply in just a few clicks.
Find JobsClinical Research Manager Jobs by City in Kansas
Where Kansas roles are concentrated, by current openings.
Clinical Research Manager 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 manager jobs across Kansas.
- Bachelor's degree in life sciences, nursing, or a related clinical field required
- Minimum two years managing clinical trials or overseeing research staff directly
- Certified Clinical Research Professional (CCRP) or CCRC credential strongly preferred
- Working knowledge of FDA regulations, GCP guidelines, and IRB submission processes
- Experience with electronic data capture systems such as REDCap or Medidata Rave
- Strong project management skills with demonstrated ability to meet protocol timelines
Clinical Research Manager Jobs in Kansas: Frequently Asked Questions
How do you become a clinical research manager in Kansas?
Most clinical research manager roles in Kansas require a bachelor's degree in a life science, nursing, or a health-related field, followed by several years of hands-on trial coordination experience. Kansas does not issue a state-specific license for this role, so the credentialing path runs through national bodies: the Society of Clinical Research Associates offers the CCRP credential, which Kansas employers widely recognize as the professional benchmark for moving into management.
Which companies hire clinical research managers in Kansas?
Kansas clinical research manager 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. Kansas's concentration of academic medical centers and pharmaceutical manufacturing facilities means hiring tends to be steady rather than cyclical, with the University of Kansas Health System and regional health networks among the most consistent sources of openings.
Which Kansas cities have the most clinical research manager jobs?
Overland Park, Topeka, and Kansas City account for the largest share of clinical research manager openings in Kansas. Wichita drives demand through its large hospital networks and growing biomedical sector, Kansas City benefits from its position as a regional healthcare hub anchored by major academic and specialty care institutions, and Lawrence draws openings connected to University of Kansas research programs and affiliated clinical partners.
Are there remote clinical research manager jobs in Kansas?
Yes, but they're limited. About 0% of clinical research manager openings tied to Kansas are remote or hybrid as of August 2026, reflecting the reality that much of the role involves on-site trial oversight, staff supervision, and IRB coordination that requires physical presence. The portions most likely to be done remotely are regulatory document review, data monitoring, and sponsor communication.
How can I get hired as a clinical research manager in Kansas with little or no experience?
The most realistic entry path is starting as a clinical research coordinator at a Kansas academic medical center or hospital system, then building toward management. The University of Kansas Health System and Wichita-area hospital networks regularly bring on research coordinators without prior management experience. Earning a CCRP credential early and moving laterally from roles like research nurse, IRB specialist, or clinical data associate gives candidates a credible foundation for promotion into managerial positions within two to four years.
Where can I find and apply to clinical research manager jobs in Kansas?
You can find and apply to clinical research manager jobs in Kansas on Migrate Mate, which lists current Kansas openings. Search the available roles, find the ones that match your experience and target location, and apply directly to the ones that fit.
See All 10 Clinical Research Manager Jobs in Kansas
Find roles in Kansas that match your experience and apply in just a few clicks.
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