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.
Senior Clinical Research Associate, Sponsor Aligned, Oncology IQVIASenior Clinical Research Associate, Sponsor Aligned, OncologyOverland Park, KansasWe create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. 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).
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 Saint Luke's Health System IncClinical Research CoordinatorKansas City, MOAs a Clinical Research Coordinator in this position, you will prepare the site for conduct of the study identify potential study participants, conduct informed consent, assist with scheduling labs and appointments, gather and record study related data, and provide patient education for various research studies. Saint Luke's Hospital in Kansas City, MO is seeking a Research Coordinator to join our research team to assist with providing and coordinating care for patients active in various research studies.
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.
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.
Clinical Research Assistant - Internal Medicine (Physical Activity and Weight Management) University of Kansas Medical CenterClinical Research Assistant - Internal Medicine (Physical Activity and Weight Management)Kansas City, MO$22.88–$33.17 / hourWithin the Division of Physical Activity and Weight Management at KUMC, Clinical Research Assistants contribute to all phases of study implementation, assist with data collection, and perform outcome assessments for a variety of physical activity, nutrition, and weight management research programs. Job Description Summary: The Clinical Research Assistant in the Department of Internal Medicine, Division of Physical Activity and Weight Management, is responsible for delivering both individual and group-based health education, exercise instruction, and exercise testing.
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, 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.
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 Assistant - Cancer Center University of Kansas Medical CenterClinical Research Assistant - Cancer CenterKS$22.88–$33.17 / hourMay 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. Job Description Summary: The Clinical Research Assistant assists in entry level clinical research activities including collecting information from patients/study participants and families.
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.
Clinical Research Nurse Coordinator The University of Kansas Health SystemClinical Research Nurse CoordinatorKansas City, KansasThe Clinical Research Nurse Coordinator focuses on patient safety and high-quality nursing care by identifying and clarifying patient needs, performing clinic related patient care, conducing health education, promoting patient advocacy, coordinating health care services, and evaluating patient outcomes. Required Licensure and Certification Licensed Registered Nurse (LRN) - Multi-State - State Board of Nursing Staff hired prior to 2/1/2024 are required to obtain a multistate RN license from the state in which they live at the time of their next RN license renewal by 4/30/2028.
Inpatient Clinical Research Nurse Coordinator The University of Kansas Health SystemInpatient Clinical Research Nurse CoordinatorKansas City, KSThe Clinical Research Nurse Coordinator focuses on patient safety and high-quality nursing care by identifying and clarifying patient needs, performing clinic related patient care, conducing health education, promoting patient advocacy, coordinating health care services, and evaluating patient outcomes. Licensed Registered Nurse (LRN) - Multi-State - State Board of Nursing Staff hired prior to 2/1/2024 are required to obtain a multistate RN license from the state in which they live at the time of their next RN license renewal by 4/30/2028.
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.
Prior Authorization Clinical Pharmacist Elevance HealthPrior Authorization Clinical PharmacistOverland Park, KansasUnless expressly allowed by state or federal law, or regulation, must be located in a state or territory of the United States when conducting utilization review or an appeals consideration and cannot be located on a US military base, vessel or any embassy located in or outside of the US, unless they are command-sanctioned activities. For URAC accredited areas, the following professional competencies apply: Associates in this role are expected to have strong oral, written and interpersonal communication skills, problem-solving skills, facilitation skills, and analytical skills.
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.