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Clinical research specialist Jobs in Kansas City, MO
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Research Compliance Specialist
The Ohio State UniversityKansas City, KS, United States- Promoted
- New!
Clinical Research Assistant - Rehab Med
University of Kansas Medical CenterKansas City, KS, United StatesClinical Informatics Specialist
The University of Kansas Health SystemShawnee Mission, KSClinical Research Coordinator - Women's Health
University HealthKansas City, MO- Promoted
- New!
Product Owner
Clinical Research IOKansas City, MO, United StatesSr Clinical Research Coordinator
Children’s MercyKansas City, MO, USSenior Clinical Research Coordinator
US Tech SolutionsOverland Park, KS- Promoted
Clinical Diabetes Specialist - Kansas City
Sequel Medical TechnologyKansas City, KS, USClinical Research Coordinator (Kansas City, MO) •
Profound Research LLCKansas City, Missouri, United States, 64101- Promoted
Clinical Training Specialist
AVITA Medical Americas, LLCKansas City, MO, USClinical Research Nurse - Cardiology
Saint Luke's Health SystemKansas City , MOMedical Research Specialist
Shook, Hardy & Bacon L.L.P.Kansas City, MO- Promoted
Clinical Research Associate
Piper CompaniesKansas, KS- Promoted
Clinical Pharmacy Specialist, Infectious Disease
Children's MercyKansas City, MO, United States- Promoted
Clinical Research Coordinator
Alcanza Clinical ResearchKansas City, MO, USClinical Research Monitor, Midwest
Edwards LifesciencesUSA, Missouri, Remote- Promoted
Clinical Nutrition Database Specialist
AdventHealthShawnee, KS, United StatesSenior Clinical Research Associate - CNS - Midwest
Worldwide Clinical TrialsKansas, USAClinical Support Specialist
Owens & Minor, Inc.Kansas City, KSResearch Compliance Specialist
The Ohio State UniversityKansas City, KS, United States- Full-time
A company is looking for a Research Compliance Specialist to support research studies through regulatory oversight and administrative assistance.Key ResponsibilitiesPrepare and submit Institutional Review Board (IRB) applications, revisions, and amendmentsCoordinate study activities, maintain lab calendar, and support conflict of interest reportingAssist with grant application processes and provide general support for study operationsRequired QualificationsBachelor's degree in a related field (e.g., health sciences, research administration)Experience with IRB submissions and regulatory processes preferredPrior experience in clinical or academic research settings is desirableA minimum of 1 year of relevant experience is preferredProficiency in Microsoft Office Suite and familiarity with research databases is a plus