Clinical Research Assistant - Otolaryngology University of Kansas Medical CenterClinical Research Assistant - OtolaryngologyKansas City, MO$22.88–$33.17 / hourThe Clinical Research Assistant works with departmental faculty, trainees, clinical teams, laboratory personnel, and research collaborators to support studies involving chronic rhinosinusitis, sinonasal inflammatory disease, environmental exposure-related airway disease, mucociliary dysfunction, epithelial and cellular biology, mucus and tissue specimens, and inflammatory or molecular biomarker research. A major focus of the position is supporting the organization and maintenance of a departmental sinonasal and upper airway tissue biobank, including patient recruitment, informed consent, clinical data collection, biospecimen acquisition, specimen processing, sample tracking, and linkage of biospecimens to relevant clinical data.
NewClinical Research Assistant - Neurology (PROMUS Lab) (Part-Time) University of Kansas Medical CenterClinical Research Assistant - Neurology (PROMUS Lab) (Part-Time)Kansas City, MO$22.88–$33.17 / hourJob Description Summary: The Department of Neurology is hiring a part-time Clinical Research Assistant (CRA) within the PoweR Of MUSic (PROMUS) to assist with several active research grants and to support future research projects in the PROMUS Lab at the University of Kansas Medical Center (KUMC). Participate in quality assurance activities by reviewing clinical data in medical record charts, assessing pharmacy compliance with protocol criteria, and reviewing study documentation to ensure compliance with GCP guidelines and FDA CFR.
Clinical Research Associate, Sponsor Dedicated IQVIA Holdings IncClinical Research Associate, Sponsor DedicatedKansas City, MO$71,900–$189,000 / yearEnsure 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.
Senior Clinical Research Associate, Sponsor Dedicated IQVIA Holdings IncSenior Clinical Research Associate, Sponsor DedicatedOverland Park, KS$74,500–$197,500 / yearEnsure 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.
Clinical Research Associate - Sponsor Dedicated IQVIA Holdings IncClinical Research Associate - Sponsor DedicatedOverland Park, KS$87,200–$182,000 / yearEnsure 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. Job Overview: Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
Clinical Research Associate, Full Service IQVIA Holdings IncClinical Research Associate, Full ServiceOverland Park, KS$49,200–$175,100 / yearEnsure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements. Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Manager Of Clinical Operations Argenta GlobalManager Of Clinical OperationsShawnee, KSCoordinate and assign tasks to clinical personnel and ensure projects are compliant with Good Clinical Practice Guidelines (if applicable) to deliver high quality data to the study Sponsors. Our teams combine deep scientific expertise with world-class manufacturing capabilities to deliver innovative therapies that improve the lives of animals around the world.
Clinical Research Coordinator - Internal Medicine (All of Us) University of Kansas Medical CenterClinical Research Coordinator - Internal Medicine (All of Us)Kansas City, MO$60,800–$91,200 / yearJob Description Summary: The Clinical Research Coordinator (CRC) supports the All of Us Research Program (AoURP) by coordinating pediatric participant enrollment and research activities across The University of Kansas Health System, the University of Kansas Medical Center, community outreach events, and local enrollment centers. Through partnerships among academic medical centers, healthcare systems, and community organizations across the Heartland region, the program collects health information and biospecimens from participants to support research on biological, environmental, behavioral, and social factors that influence health and disease.
Clinical Research Associate (CRA II/Senior) - Oncology - US Any Region Parexel International CorpClinical Research Associate (CRA II/Senior) - Oncology - US Any RegionKSWith 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere. As a CRA, you will manage clinical sites from identification through closeout, serving as the primary point of contact for site teams and helping ensure study quality, patient safety, regulatory compliance, and accurate clinical data.
Clinical Research Associate (CRA II/Senior) - Metabolic - US Any Region Parexel International CorpClinical Research Associate (CRA II/Senior) - Metabolic - US Any RegionKSWith 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere. As a CRA, you will manage clinical sites from identification through closeout, serving as the primary point of contact for site teams and helping ensure study quality, patient safety, regulatory compliance, and accurate clinical data.
Clinical Research Associate (CRA II/Senior) - Ophthalmology - US Any Region Parexel International CorpClinical Research Associate (CRA II/Senior) - Ophthalmology - US Any RegionKSWith 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere. As a CRA, you will manage clinical sites from identification through closeout, serving as the primary point of contact for site teams and helping ensure study quality, patient safety, regulatory compliance, and accurate clinical data.
Clinical Research Coordinator HCA Healthcare IncClinical Research CoordinatorOverland Park, KSProvide/coordinate the highest level of contact, counseling and support services Coordinate study activities and patient care with medical staff Implement and adhere to study protocol Perform Phlebotomy and IV procedures Prepare laboratory specimens for analysis, monitoring tests and procedures, shipping frozen specimen Execute medical orders within parameters of education, training and licensure Conduct study activities helping to ensure all safety parameters Maintain patient records in EMR and appropriate hospital records Assess and report adverse study events, including the IRB and any research sponsors Complete all paperwork affiliated with the study, including but not limited to the requirements of the facility, the IRB and the study Sponsor. Assess each proposed study protocol Facilitate administrative review and approval of proposed studies Develop tactical study procedures Develop any necessary study documents not provided by sponsor or IRB Educate HCA staff regarding research and study protocols Screen and recruit patients based on protocol criteria Explain study protocols, procedures and treatments to patients and families Conduct the Informed Consent process in conjunction with study investigators Ensure that an original copy of any subjects Informed Consent Document is the in the research binders, as well as, a copy on the subject's medical record.
Overland Park, TX- Clinical Research Nurse Actalent IncOverland Park, TX- Clinical Research NurseOverland Park, KS$25–$35 / hourWe are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
NewCommunity Health Worker / Clinical Research Assistant - Family Medicine University of Kansas Medical CenterCommunity Health Worker / Clinical Research Assistant - Family MedicineKansas, KS$22.88–$33.17 / hourPromote participant self-advocacy and engagement in healthcare by helping participants identify and communicate questions, concerns, and priorities; prepare for healthcare visits; navigate healthcare and community systems; and connect with appropriate services and resources. Job Description Summary: The University of Kansas Medical Center (KUMC) Department of Family Medicine and Community Health seeks a part-time Community Health Worker (CHW)/Clinical Research Assistant (CRA) to support the Securing American Indian Futures through E-Health (SAFE) study.
NewClinical Quality Program Manager Elevance Health IncClinical Quality Program ManagerOverland Park, KSCandidates should possess exceptional organizational, project management, and communication skills, with demonstrated ability to manage multiple priorities, coordinate across diverse stakeholder groups, and drive complex initiatives to successful completion. Minimum requirements: Requires a BS in health administration, nursing, or a related clinical field; 4 years of health care quality or data analysis experience; or any combination of education and experience, which would provide an equivalent background.
Clinical Research Coordinator Actalent IncClinical Research CoordinatorOverland Park, KS$25–$35 / hourWe are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
Registered Nurse Clinical Research HCA Healthcare IncRegistered Nurse Clinical ResearchOverland Park, KSWith a focus on meeting the needs of our patients at all access points, Physician Services is dedicated to implementing innovative, physician-driven, value-added solutions to assist physicians in providing high-quality, patient-centered care, aligning with our mission to care for and enhance human life. Supporting HCA Healthcare's 186 hospitals and 2,400+ sites of care, Physician Services plays a crucial role as the main entry point for patients looking for high-quality healthcare within the HCA Healthcare system.
Clinical Research Specialist Actalent IncClinical Research SpecialistOverland Park, KS$19.50–$22 / hourThe setting includes typical clinical and laboratory equipment such as centrifuges, sample storage units, and computer workstations, and requires adherence to facility procedures and professional conduct appropriate for a clinical research environment. This role is based inside a clinical research facility in Overland Park, KS, with the Clinical Research Specialist stationed just off the clinic floor and working closely with the adjacent laboratory.
Clinical Research Coordinator, On-Site IQVIA Holdings IncClinical Research Coordinator, On-SiteKansas City, MO$37,800–$94,500 / yearJoin Avacare, a dynamic Site Management Organization (SMO) where Clinical Research Coordinators (CRCs) gain unparalleled exposure to diverse trials, hands-on responsibilities, and a collaborative team environment. You'll gain experience across multiple therapeutic areas, manage complex protocols, and take ownership of key trial activities - from patient recruitment and informed consent to regulatory documentation and site audits.
Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health IncExperienced Clinical Research Associate - Sponsor DedicatedKSTogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.