Research Jobs in Kansas City, MO
Research jobs in Kansas City are in steady demand, concentrated in the Crossroads, Crown Center, and the University of Kansas City corridor across healthcare, life sciences, and applied social research. Employers hiring right now include University of Kansas Medical Center, University of Missouri-Kansas City, and Children's Mercy Hospitals & Clinics. Scan the live roles below and apply to whichever ones fit.
Find Research JobsOverview
Showing 5 of 48+ Research jobs
Job Overview
Work as an integral member of investigator site staff managing the day-to-day coordination and execution of clinical studies in accordance with the protocol, contracted scope of work, good clinical practice, sponsor and standard operating procedures (SOPs) and any relevant local guidelines and regulations.
- Provide clinical research support to investigators to prepare for and execute assigned research studies
- Review study protocols, source document forms, other study-specific documents, and electronic data capture systems used to record clinical research data
- Collect and submit regulatory/ethics documentation as required by the Federal Drug Administration (FDA) and other regulatory bodies governing the conduct of the study
- Recruit and screen patients for clinical trials and maintain subject screening and enrollment logs
- Orient research subjects to the study including the purpose of the study, procedures and protocol requirements such as timeline for visits
- Maintain source documentation based on protocol requirements that adhere to Good Clinical Practice (GCP)/International Conference on Harmonization (ICH) documentation principles
- Schedule and execute study visits and perform study procedures as delegated and supervised by the Principal Investigator
- Handle lab testing and analysis including preparation of specimen collection tubes and lab logistics
- Monitor subject safety and reports adverse events and reactions to Principal Investigator, study team members and IRBs as appropriate
- Correspond with research subjects to troubleshoot study-related questions or concerns
- Participate in routine meetings with site study staff and Investigators to confirm study tasks are assigned and are executed to the expected standards
- Actively involved in study data quality checking and query resolution
- Perform a variety of complex clinical research procedures including but not limited to electrocardiogram (ECG), lab sample collection, spirometry, vital signs, dose verifications, cardiac telemetry monitoring, and questionnaire administration
- Assist investigator in verifying that research study objectives are met on time, within budget and according to application protocol requirements, clinical research regulations and quality standards
- Assist in providing training to new investigator site staff members on study-specific topics and requirements
- Maintain adherence to investigator site staff training requirements by auditing and maintaining training records
- Prepare for and as needed attends study monitoring visits, study audits and regulatory inspections with clinical research regulatory agencies
- Adhere to standard operating procedures (SOPs) and other directives throughout the process
- Assist research site with coverage planning related to staffing and scheduling for research projects
- Degree in health care or other scientific discipline preferred
- 3 years' experience as Site Clinical Research Coordinator as accepted in accordance with local country requirements. Equivalent combination of education, training and experience.
- Sound knowledge of clinical trials.
- Advanced knowledge of the principals of Good Clinical Practices (GCP).
- In-depth knowledge of protocol and study-specific operating procedures, consent forms, and study schedules.
- Sound knowledge of medical terminology.
- Ability to prioritize, seek input, problem solve and work in a team environment.
- Ability to maintain confidentiality.
- Ability to establish and maintain effective working relationships with coworkers, managers and clients.
- Applicable certifications and licenses as required by country, state, and/or other regulatory bodies.
- Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) strongly preferred.
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 $62,800.00 - $157,100.00. 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.Job Overview
Work as an integral member of investigator site staff managing the day-to-day coordination and execution of clinical studies in accordance with the protocol, contracted scope of work, good clinical practice, sponsor and standard operating procedures (SOPs) and any relevant local guidelines and regulations.
- Provide clinical research support to investigators to prepare for and execute assigned research studies
- Review study protocols, source document forms, other study-specific documents, and electronic data capture systems used to record clinical research data
- Collect and submit regulatory/ethics documentation as required by the Federal Drug Administration (FDA) and other regulatory bodies governing the conduct of the study
- Recruit and screen patients for clinical trials and maintain subject screening and enrollment logs
- Orient research subjects to the study including the purpose of the study, procedures and protocol requirements such as timeline for visits
- Maintain source documentation based on protocol requirements that adhere to Good Clinical Practice (GCP)/International Conference on Harmonization (ICH) documentation principles
- Schedule and execute study visits and perform study procedures as delegated and supervised by the Principal Investigator
- Handle lab testing and analysis including preparation of specimen collection tubes and lab logistics
- Monitor subject safety and reports adverse events and reactions to Principal Investigator, study team members and IRBs as appropriate
- Correspond with research subjects to troubleshoot study-related questions or concerns
- Participate in routine meetings with site study staff and Investigators to confirm study tasks are assigned and are executed to the expected standards
- Actively involved in study data quality checking and query resolution
- Perform a variety of complex clinical research procedures including but not limited to electrocardiogram (ECG), lab sample collection, spirometry, vital signs, dose verifications, cardiac telemetry monitoring, and questionnaire administration
- Assist investigator in verifying that research study objectives are met on time, within budget and according to application protocol requirements, clinical research regulations and quality standards
- Assist in providing training to new investigator site staff members on study-specific topics and requirements
- Maintain adherence to investigator site staff training requirements by auditing and maintaining training records
- Prepare for and as needed attends study monitoring visits, study audits and regulatory inspections with clinical research regulatory agencies
- Adhere to standard operating procedures (SOPs) and other directives throughout the process
- Assist research site with coverage planning related to staffing and scheduling for research projects
- Degree in health care or other scientific discipline preferred
- 3 years' experience as Site Clinical Research Coordinator as accepted in accordance with local country requirements. Equivalent combination of education, training and experience.
- Sound knowledge of clinical trials.
- Advanced knowledge of the principals of Good Clinical Practices (GCP).
- In-depth knowledge of protocol and study-specific operating procedures, consent forms, and study schedules.
- Sound knowledge of medical terminology.
- Ability to prioritize, seek input, problem solve and work in a team environment.
- Ability to maintain confidentiality.
- Ability to establish and maintain effective working relationships with coworkers, managers and clients.
- Applicable certifications and licenses as required by country, state, and/or other regulatory bodies.
- Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) strongly preferred.
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 $62,800.00 - $157,100.00. 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.See All 48 Research Jobs in Kansas City
Find roles in Kansas City that match your experience and apply in just a few clicks.
Find Research JobsResearch Job Market in Kansas City
Who's Hiring
- University of Kansas Medical Center18
- University of Missouri-Kansas City11
- Children's Mercy Hospitals & Clinics4
- IQVIA2
- Stowers Institute for Medical Research2
Top Industries Hiring
- Healthcare & Medical Services15
- Education8
- Medical Devices1
- Accounting & Auditing1
- Banking & Financial Services1
Research Jobs in Kansas City: Frequently Asked Questions
How do I get a research job in Kansas City?
Research roles in Kansas City cluster in healthcare systems, pharmaceutical and biotech firms, university-affiliated institutes, and applied social policy organizations. Candidates who do well here typically bring hands-on data collection or analysis experience relevant to one of those sectors. Familiarity with the Kansas City research corridor, from the medical center area to the Crossroads innovation community, helps you target applications where demand is actually concentrated rather than applying broadly.
Which companies hire researchs in Kansas City?
Employers hiring researchs in Kansas City right now include University of Kansas Medical Center, University of Missouri-Kansas City, and Children's Mercy Hospitals & Clinics, based on current listings on Migrate Mate as of July 2026. Kansas City's hiring landscape includes large health systems, contract research organizations, federal agency satellite offices, and regional nonprofits conducting community and policy research.
Are there remote research jobs in Kansas City?
Yes, though it depends heavily on the type of work: desk-based and analytical roles tend to go remote far more often than fieldwork, clinical, or lab positions. About 10% of research openings tied to Kansas City are remote or hybrid as of July 2026, with literature review, data analysis, and policy research roles representing the largest share of those flexible arrangements.
How can I get a research job in Kansas City with little or no experience?
The most realistic entry point in Kansas City is a research coordinator or research assistant role at one of the area's major health systems or university-affiliated research centers, which regularly hire candidates still building their credentials. Volunteering with local nonprofits conducting community needs assessments or policy work is another concrete path. Highlighting any IRB training, survey tools experience, or coursework in statistics gives you a visible edge over candidates with comparable backgrounds.
Which industries hire the most researchs in Kansas City?
Kansas City research roles concentrate in Healthcare & Medical Services, Education, and Medical Devices, based on current listings on Migrate Mate as of July 2026. Kansas City's strength as a regional healthcare hub and its growing life sciences and applied social research sectors drive consistent local demand for research professionals across both clinical and non-clinical settings.
Related Jobs in Missouri
See All 48 Research Jobs in Kansas City
Find roles in Kansas City that match your experience and apply in just a few clicks.
Find Research Jobs