NewClinical Research Associate (CRA 2), Sponsor Dedicated IQVIAClinical Research Associate (CRA 2), Sponsor DedicatedOverland Park, KansasEnsure 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 Associate - Sponsor Dedicated IQVIAClinical Research Associate - Sponsor DedicatedOverland Park, KansasEnsure 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.
Per Diem Clinical Research Nurse - Home Visits Science 37Per Diem Clinical Research Nurse - Home VisitsKansas City, MO$50–$55 / hourWith interest/expertise in Science 37's decentralized model of care delivery, the Mobile Research Nurse will perform delivery of care to participants as well as collaborate with brick and mortar sites, if indicated, for shared clinical trial implementation. Science 37's Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials.
Phlebotomist - Clinical Research Technician II AltasciencesPhlebotomist - Clinical Research Technician IIOverland Park, KansasBy living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives.
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.
Clinical Research Coordinator Act for HealthClinical Research CoordinatorKansas City, KansasParticipates in recruitment of participants to include personally engaging the general public face to face in local across hard-to-reach communities, attending community events, speaking with physicians and people across diverse cultures and backgrounds to support meeting participant enrollment targets. Ensures adherence to clinical trial protocols and supports the clinical trials team in ensuring that trials are conducted and comply with all regulatory, state, national and internationally accepted guidelines for Good Clinical Practice (ICH GCP).
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, On-Site IQVIAClinical Research Coordinator, On-SiteKansas City, MissouriJoin 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.
Clinical Research Coordinator HCA HealthcareClinical Research CoordinatorOverland 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 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.
NewNeonatologist – Clinical Research Children's Mercy Hospital (MO)Neonatologist – Clinical ResearchKansas City, MOThe Neonatology Division at Children’s Mercy Hospital Kansas City is seeking a board-certified Neonatologist to provide clinical care in community Level III Neonatal Intensive Care Units and our regional referral Level IV NICU. The Home Ventilator Program and the Infant Lung Center provide a candidate with interest in infant chronic lung disease rich opportunity for participation in clinical follow up and research of such infants.
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).
Clinical Sales Specialist, Electrophysiology - LAAO (Kansas City, MO) AbbottClinical Sales Specialist, Electrophysiology - LAAO (Kansas City, MO)Kansas City, Missouri$68,000–$136,000 / yearIn this role, the Clinical Specialist with train interventional cardiologists, catheter lab staff and ancillary personnel on the use of Structural Heart products and provide technical support to physicians during procedures. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines.
Clinical Research Assistant II Children's Mercy KCClinical Research Assistant IIKansas City, MissouriRemoteFull timeWe know that our greatest strengths come from the people who make up our team, so we hire great people from a wide variety of backgrounds, not just because it’s the right thing to do, but because it makes our hospital stronger and our patient care more compassionate. New employees must be willing to be vaccinated if found non-immune to measles, mumps, rubella (MMR) and chicken pox (varicella) and/or without evidence of tetanus, diphtheria, acellular pertussis (Tdap) vaccination since 2005.
NewFSP 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 IRESenior Clinical Research AssociateKansas City, MissouriSenior Clinical Research Associate - Cardio (Smart Pulse A-fib) - All Regions ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. The ideal candidate will have cardiovascular medical device monitoring experience- however, cardiovascular/electrophysiology pharma monitoring experience will be considered.
Clinical Program Manager - Trauma The University of Kansas Health SystemClinical Program Manager - TraumaKansas City, KansasOversees the Trauma Registry and Trauma Performance Improvement Program by directing data collection, analysis, reporting, and submission to state and national databases; developing and monitoring performance improvement indicators; collaborating with quality teams and Trauma Registrars; and ensuring effective identification of issues, follow-up, and loop closure. The Trauma Program Manager oversees the trauma service, including supervision of staff, coordination of trauma activities and patient flow, and advancement of optimal trauma care through clinical operations, professional and community education, research, performance improvement, and administrative functions.
NewResearch Project Manager - Comprehensive Integrated Research Operations (CIRO) University of Kansas Medical CenterResearch Project Manager - Comprehensive Integrated Research Operations (CIRO)Kansas City, MO$92,800–$139,200 / yearThe position coordinates project activities among investigators, study teams, sponsors, and institutional stakeholders; monitors project timelines, budgets, and reporting requirements; and supports the implementation of operational processes across the research enterprise. Perform clinical research duties, as needed, to support study operations at any level from Clinical Research Assistant through Clinical Research Supervisor, including participant assessments, informed consent, specimen processing, and protocol-required study procedures.
Clinical Research Coordinator Saint Luke's Health System Kansas CityClinical 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.