NewQuality Assurance Leader for Early Phase Clinical Research AltasciencesQuality Assurance Leader for Early Phase Clinical ResearchOverland Park, KansasThe Manager, Quality Assurance also supports inspection readiness, quality issue escalation, staff development, and the effective execution of QA programs within the assigned site, function, or business area. The Manager, Quality Assurance is responsible for leading QA staff, resources, and assigned QA activities to ensure effective quality oversight, timely execution, and compliance with applicable internal procedures and external regulatory requirements.
Senior Clinical Research Associate IRESenior Clinical Research AssociateKansas City, MissouriThe ideal candidate will have cardiovascular medical device monitoring experience- however, complex experience in cardiovascular/electrophysiology pharma monitoring and/or Coordinator/Nursing experience will be considered. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Clinical Research Physician - Dermatologist (Part Time) Alcanza Clinical ResearchClinical Research Physician - Dermatologist (Part Time)Kansas City, MissouriEssential Job Duties: Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes. The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes.
Clinical Research Physician - Internal Medicine (Part time) Alcanza Clinical ResearchClinical Research Physician - Internal Medicine (Part time)Kansas City, MOEssential Job Duties: Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes. The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes.
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 Nurse Coordinator - Neurology (Huntington Disease) University of Kansas Medical CenterClinical Research Nurse Coordinator - Neurology (Huntington Disease)Kansas City, MO$70,200–$105,300 / yearJob Description Summary: The Clinical Research Nurse Coordinator in the Department of Neurology works closely with various clinical staff members and researchers of the University of Kansas Health System (TUKHS), KU Medical Center (KUMC) and Huntington Disease (HD) Clinic to identify potential study participants and to provide care for people with HD and their families in the HD Clinic. Oversee post-award grant and contract administration, including processing purchase orders, preparing invoices to sponsors, tracking expenditures, reviewing award budgets with investigators, and ensuring financial and compliance alignment.
Senior Clinical Research Coordinator - Cancer Center University of Kansas Medical CenterSenior Clinical Research Coordinator - Cancer CenterKS$70,200–$105,300 / yearJob Description Summary: The Senior Clinical Research Coordinator works collaboratively with multidisciplinary teams, research, and hospital staff to recruit, screen, educate, and assist in the overall clinical study coordination of clinical research. The Senior Clinical Research Coordinator will manage assigned clinical research studies by supervising a variety of complex activities involved in the collection, compilation, documentation, and analysis of clinical research data.
Clinical Research Associate, Sponsor Dedicated, IQVIA IQVIA Holdings IncClinical Research Associate, Sponsor Dedicated, IQVIAOverland Park, KS$71,900–$182,000 / 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.
Senior Regulatory Coordinator - Comprehensive Integrated Research Operations (CIRO) University of Kansas Medical CenterSenior Regulatory Coordinator - Comprehensive Integrated Research Operations (CIRO)Kansas City, MO$60,800–$91,200 / yearJob Description Summary: The Senior Regulatory Coordinator within the Comprehensive Integrated Research Operations (CIRO) department serves as the administrative resource and liaison involved in supporting the business aspects of the clinical research enterprise. The Senior Regulatory Coordinator is responsible for leading and performing study-specific regulatory and safety reporting for a group of investigators, within multiple cost centers in the Department of Internal Medicine.
FSP Clinical Research Associate 2 - Central Region Fortrea IncFSP Clinical Research Associate 2 - Central RegionKSRemote$100,000–$112,000 / yearResponsibilities: Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.
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.
Senior Clinical Research Associate ICON PlcSenior Clinical Research AssociateLawrence, KSRemoteICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Clinical Research Associate, Sponsor Dedicated IQVIA Holdings IncClinical Research Associate, Sponsor DedicatedOverland Park, KS$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.
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.
Research Assistant - Internal Medicine (Endocrinology, Metabolism & Genetics) University of Kansas Medical CenterResearch Assistant - Internal Medicine (Endocrinology, Metabolism & Genetics)Kansas City, KS$22.88–$33.17 / hourhttps://kumc.wd5.myworkdayjobs.com/en-US/kumc-jobs/job/Kansas-City-Metro-Area/Research-Assistant---Internal-Medicine--Endocrinology--Metabolism---Genetics-_JR009846](https://apptrkr.com/7084484). [https://www.kumc.edu/human-resources/benefits.html](https://apptrkr.com/get_redirect.php?id=7084484&targetURL=https://www.kumc.edu/human-resources/benefits.html){target="_blank".
Clinical Research Coordinator - Neurology (Neuromuscular) University of Kansas Medical CenterClinical Research Coordinator - Neurology (Neuromuscular)Fairway, KS$60,800–$91,200 / yearAssists physician in cerebrospinal fluid (CSF) collection for clinical trials by educating patient / caregiver regarding the lumbar puncture procedure, preparing lumbar puncture supplies, providing supplies to physician during procedure while maintaining sterile field, aliquoting CSF by protocol-specified amounts into separate vials for storage and transport, instructing patient/caregiver in post-lumbar puncture care and expectations, conducting follow -up phone call to determine if any adverse events were experienced. Coordinates of all aspects of study visit activities for patients and families, including scheduling of hospital-based procedures such as MRI and PET, and other procedures to include clinical study visit interviews and assessments, ECG, lab draws, IV infusions, lumbar punctures, and dispensation of study medication.
Research Assistant - Sleep Neurobiology, Biological and Biomedical Systems, UMKC School of Science and Engineering University of Missouri-Kansas CityResearch Assistant - Sleep Neurobiology, Biological and Biomedical Systems, UMKC School of Science and EngineeringKansas City, MOIn particular, the successful candidate will employ a variety of techniques, including Drosophila genetics, behavioral assays, confocal microscopy, live-brain imaging and neural circuits mapping and manipulation, to identify the molecular mechanisms used by VNC-SP neurons to regulate sleep as well as their presynaptic inputs and postsynaptic partners. We have recently identified two new sleep-promoting neurons located in the fly equivalent of the spinal cord, the ventral nerve cord (VNC) ( https://journals.plos.org/plosbiology/article?id=10.1371/journal.pbio.3002012 ).
ASSISTANT/ASSOCIATE PROFESSOR Nursing & Health Studies, Tenure-Eligible / UMKC School of Nursing & Health Studies / Research Education University of Missouri-Kansas CityASSISTANT/ASSOCIATE PROFESSOR Nursing & Health Studies, Tenure-Eligible / UMKC School of Nursing & Health Studies / Research EducationKansas City, MOUMKC provides unique opportunities for research and health care collaboration across its Schools of: Medicine, Dentistry, Nursing and Health Studies, and Pharmacy as well as University Health physicians, regional health care institutions, and the University of Missouri System's NextGen Data Science and Analytics Innovation Center. A program of research focus that aligns with the Schools strategic priorities in innovative nursing education, clinical/biological research, or health systems and outcomes research, with a focus on improving the health of vulnerable, underserved, or urban populations.
Clinical Trial Fiscal Analyst- Research Administration University of Kansas Medical CenterClinical Trial Fiscal Analyst- Research AdministrationKansas City, MO$60,800–$91,200 / yearPerform comprehensive and independent review of various clinical trial documents such as budgets, contracts, protocols and consent forms for compliance and billing purposes, and review accounts for discrepancies and reconcile differences. Prepare, examine and analyze accounting records and other financial reports to assess accuracy and completeness according to proposed budgets and compliance with contracts with sponsoring entities.
Research Assistant - Sleep Neurobiology, Biological and Biomedical Systems, UMKC School of Science and Engineering University of MissouriResearch Assistant - Sleep Neurobiology, Biological and Biomedical Systems, UMKC School of Science and EngineeringKansas City, MOIn particular, the successful candidate will employ a variety of techniques, including Drosophila genetics, behavioral assays, confocal microscopy, live-brain imaging and neural circuits mapping and manipulation, to identify the molecular mechanisms used by VNC-SP neurons to regulate sleep as well as their presynaptic inputs and postsynaptic partners. We have recently identified two new sleep-promoting neurons located in the fly equivalent of the spinal cord, the ventral nerve cord (VNC) ( https://journals.plos.org/plosbiology/article?id=10.1371/journal.pbio.3002012 ).