NewRegistered Nurse Clinical Research Kansas City Card Arrhythmia ResearchRegistered 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 Assistant - Cancer Center University of Kansas Medical CenterClinical Research Assistant - Cancer CenterWestwood East, KS$22.88–$33.17 / hourJob Description Summary: Under general supervision, the Clinical Research Assistant will work with multidisciplinary teams including patients/study participants, families, physicians, administrative staff, and sponsor and CRO representatives to coordinate all aspects of clinical research. At the University of Kansas Medical Center, a reasonable estimate for the starting pay range will be the minimum to midpoint of the posted range, taking into account the combination of factors listed above.
Clinical Research Assistant (Part-Time) - Pediatrics University of Kansas Medical CenterClinical Research Assistant (Part-Time) - PediatricsKansas City, MO$22.88–$33.17 / hourThe Clinical Research Assistant will facilitate participant recruitment and enrollment, data collection and entry, and other duties related to pediatric research for projects addressing topic areas such as vaccination rates, mental health service access and improving child health. Provide study onboarding to participants who have been recruited, which may involve scheduling onboarding meetings, and assisting with onboarding presentations.
NewClinical Research Assistant I Children's Mercy KCClinical Research Assistant IKansas City, MissouriUnder the direct supervision of a Research Manager, the Clinical Research Assistant I will assist research team members by performing basic study procedures, and completing assigned tasks such as nasal swab collection/handling, and data collection and processing in schools. We 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.
Clinical Research Assistant - Physical Medicine & Rehabilitation University of Kansas Medical CenterClinical Research Assistant - Physical Medicine & RehabilitationKansas City, MO$22.88–$33.17 / hourJob Description Summary: The Clinical Research Assistant (CRA) in the Division of Physical Medicine and Rehabilitation assists in entry-level clinical research activities including collecting information from participants and families. At the University of Kansas Medical Center, a reasonable estimate for the starting pay range will be the minimum to midpoint of the posted range, taking into account the combination of factors listed above.
Clinical Research Assistant - Neurology (Parkinson''''s Disease Center) University of Kansas Medical CenterClinical Research Assistant - Neurology (Parkinson''''s Disease Center)Kansas City, KS$22.88–$33.17 / hourJob Description Summary: The Clinical Research Assistant in the Neurology Parkinson's Disease Center is responsible for scheduling, recruitment, evaluation, education of patients for clinical trials, documentation, and assisting the research team. At the University of Kansas Medical Center, a reasonable estimate for the starting pay range will be the minimum to midpoint of the posted range, taking into account the combination of factors listed above.
Clinical Research Coordinator- Cardiology University of Kansas Medical CenterClinical Research Coordinator- CardiologyKansas City, MO$60,800–$91,200 / yearJob Description Summary: The Clinical Research Coordinator in the department of Cardiology works collaboratively with multidisciplinary teams, research, and hospital staff in the overall clinical study coordination of clinical research. 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 Lab Technician - Internal Medicine Research University Health.Clinical Research Lab Technician - Internal Medicine ResearchUniversity Health 4 (UH4), MOMust qualify as a General Medical Laboratory Scientist under CLIA-88 through one of the following: Bachelor's degree in a chemical, physical, biological, clinical laboratory, or medical technology science field; or actively enrolled in an accredited Medical Laboratory Scientist program, OR Associate degree in a laboratory science or medical laboratory scientist program, OR Previously qualified or eligible to qualify as a generalist prior to February 29, 1992 under 42 CFR 493.1427 (3/14/90). In this dynamic role, you'll partner with investigators, research coordinators, laboratory staff, and healthcare professionals to support innovative research that helps shape the future of medicine.
Senior Research Associate or Senior Research Assistant, Maternal and Child Health, UMKC Institute for Human Development University of Missouri-Kansas CitySenior Research Associate or Senior Research Assistant, Maternal and Child Health, UMKC Institute for Human DevelopmentKansas City, MO$68,000–$80,000 / yearThis role may manage multiple projects concurrently, aligning projects, managing day-to-day operations, ensuring high-quality product or outcome delivery, managing project timelines, and collaborating with teammates and external partners to drive measurable impact. The successful candidate will demonstrate relevant training and experience that provides the following knowledge, abilities, and skills: Three or more years of experience with community-based research project management and outcome dissemination.
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.
Clinical Research Coordinator - Women''''s Health Department University Health.Clinical Research Coordinator - Women''''s Health DepartmentKansas City, MOResponsible for performing diverse administrative and clinical responsibilities requiring some analysis, sound judgment, and a high level of knowledge of specific research study protocols, Good Clinical Practice Guidelines, Federal research regulations, and institutional requirements. Responsible for coordination and management of clinical study protocols and along with the research investigator, manages many aspects of the clinical trial and conducts all research activities within an ethically based framework in accordance with federal, state, and local regulations.
Clinical Research Supervisor - Internal Medicine (All of Us Research Program) University of Kansas Medical CenterClinical Research Supervisor - Internal Medicine (All of Us Research Program)Kansas City, MO$80,600–$120,900 / yearJob Description Summary: The Clinical Research Supervisor supports the All of Us Research Program Heartland Consortium at the University of Kansas Medical Center by leading and contributing to enrollment, engagement, and data collection of pediatric and adult research participants. Monitor and drive progress toward enrollment targets, including approximately 700 pediatric participants annually, and implement strategies to address gaps.
Research Assistant Professor - Internal Medicine (Physical Activity and Weight Management) University of Kansas Medical CenterResearch Assistant Professor - Internal Medicine (Physical Activity and Weight Management)Kansas City, MOIt also supports a medically supervised weight management clinic that provides robust clinical research programs for individuals seeking weight management and health enhancement (Kansas Weight Management Programs, KWMP). Required Qualifications: Education: PhD or equivalent in energy balance, obesity prevention and treatment, exercise physiology, exercise behavior, psychology, nutrition, public health, epidemiology, or a related field relevant to weight management.
Research Assistant - Surgical Innovation Lab - UMKC School of Medicine University of MissouriResearch Assistant - Surgical Innovation Lab - UMKC School of MedicineKansas City, MO$20–$22 / hourThe Surgical Innovation Lab ("SurgiLab") is dedicated to improving surgical safety and education by addressing errors through innovative techniques, communication research, and human factors analysis. The ideal candidate will have excellent time management and organizational abilities, strong written and verbal communication skills, and a bachelor's degree in STEM or another relevant field.
Research Support Assistant AdventHealthResearch Support AssistantShawnee Mission, KS$20.95–$38.96 / hourLicenses and Certifications: American Association Medical Assistants (CMA [Preferred] OR Clinical Medical Assistant Certification (CMAC [Preferred] OR Registered Medical Assistant (RMA [Preferred] OR National Certified Medical Assistant (NCMA [Preferred] OR Certified Clinical Medical Assistant (CCMA [Preferred] OR Nationally Registered Certified Medical Assistant (NRCMA [Preferred]. Additional Information: An equivalent combination of education and relevant work experience may be considered in lieu of the stated degree requirement: Associates degree OR.
Research Support Assistant (Candidate MUST live within the KC Metro Area to be considered AdventHealthResearch Support Assistant (Candidate MUST live within the KC Metro Area to be consideredShawnee Mission, KS$20.95–$38.96 / hourLicenses and Certifications: American Association Medical Assistants (CMA [Preferred] OR Clinical Medical Assistant Certification (CMAC [Preferred] OR Registered Medical Assistant (RMA [Preferred] OR National Certified Medical Assistant (NCMA [Preferred] OR Certified Clinical Medical Assistant (CCMA [Preferred] OR Nationally Registered Certified Medical Assistant (NRCMA [Preferred]. Additional Information: An equivalent combination of education and relevant work experience may be considered in lieu of the stated degree requirement: Associates degree OR.
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 Alcanza Clinical Research LLCClinical Research CoordinatorKansas City, MOScheduling subjects for study visits and conducts appointment reminders; Building/updating source as needed; Conducting monitoring visits and resolves issues as needed in a timely manner; Ensuring study related reports and patient results are reviewed by investigator in a timely manner; Filing SAE/Deviation reports to Sponsor and IRB as needed; Documenting and reporting adverse events; Reporting non-compliance to appropriate staff in timely manner; Maintaining positive and effective communication with clients and team members; Always practicing ALCOAC principles with all documentation; May assist with study recruitment, patient enrollment, and tracking as needed; Maintaining confidentiality of patients, customers and company information, and; Performing all other duties as requested or assigned. Responsibilities may include but are not limited to: Screening of patients for study enrollment; Patient consents; Patient follow-up visits; Documenting in source clinic charts; Entering data in EDC and answers queries; Obtaining vital signs and ECGs; May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; Requesting and tracking medical record requests; Updating and maintaining logs, chart filings; Maintaining & ordering study specific supplies;].
Clinical Research Nurse I ICON PlcClinical Research Nurse ILenexa, KSThis role performs core nursing tasks (vitals, IVs, EKGs, injections, dosing, blood draws), and adheres to clinical research protocols that vary by trial. The Clinical Research Nurse supports the safe, compliant execution of Phase 1 clinical trials with healthy volunteers in an on-site clinic setting.
Research Assistant - Surgical Innovation Lab - UMKC School of Medicine University of Missouri-Kansas CityResearch Assistant - Surgical Innovation Lab - UMKC School of MedicineKansas City, MO$20–$22 / hourThe Surgical Innovation Lab ("SurgiLab") is dedicated to improving surgical safety and education by addressing errors through innovative techniques, communication research, and human factors analysis. The ideal candidate will have excellent time management and organizational abilities, strong written and verbal communication skills, and a bachelors degree in STEM or another relevant field.
Clinical Research Nurse - Oncology Saint Luke's Health System IncClinical Research Nurse - OncologyKansas City, MOThe Clinical Research Nurse works with the PI, department, sponsor, and institution to support and provide guidance on the administration, compliance, financial, required personnel and other aspects of clinical studies . Responsible for data entry, data query resolution in clinical study database, as well as other study-specific system management for assigned studies.
Medical Research Associate (Phlebotomist) ICON PlcMedical Research Associate (Phlebotomist)Lenexa, KSAs a Medical Research Associate/Phlebotomist at ICON, you will be responsible for meeting/greeting clinical research volunteers as they come into the clinic, checking their vitals (height, weight, blood pressure, BMI). Preferred Background: Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician backgrounds are highly desired.
Senior Clinical Research Associate - Oncology - Central - Remote Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - Oncology - Central - RemoteKSRemote$97,000–$193,000 / yearTypically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.
NewClinical 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 Saint Luke's Health System IncClinical Research NurseKansas City, MOThe Clinical Research Nurse works with the PI, department, sponsor, and institution to support and provide guidance on the administration, compliance, financial, required personnel and other aspects of clinical studies. Applicable Experience: • 2 years Registered Nurse (MO) Multi-State - National Council of State Boards of Nursing (NURSYS) • Registered Nurse (MO) - National Council of State Boards of Nursing (NURSYS).
Clinical Research Nurse (PRN) ICON PlcClinical Research Nurse (PRN)Lenexa, KSFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Join ICON as a Clinical Research Nurse, where your work supports scientific progress and helps bring innovative therapies to patients who need them.
Clinical Research Coordinator Alcanza Clinical ResearchClinical Research CoordinatorKansas city, MissouriScheduling subjects for study visits and conducts appointment reminders; Building/updating source as needed; Conducting monitoring visits and resolves issues as needed in a timely manner; Ensuring study related reports and patient results are reviewed by investigator in a timely manner; Filing SAE/Deviation reports to Sponsor and IRB as needed; Documenting and reporting adverse events; Reporting non-compliance to appropriate staff in timely manner; Maintaining positive and effective communication with clients and team members; Always practicing ALCOAC principles with all documentation; May assist with study recruitment, patient enrollment, and tracking as needed; Maintaining confidentiality of patients, customers and company information, and; Performing all other duties as requested or assigned. Responsibilities may include but are not limited to:Screening of patients for study enrollment; Patient consents; Patient follow-up visits; Documenting in source clinic charts; Entering data in EDC and answers queries; Obtaining vital signs and ECGs; May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; Requesting and tracking medical record requests; Updating and maintaining logs, chart filings; Maintaining & ordering study specific supplies;].
Budget Analyst - Comprehensive Integrated Research Operations University of Kansas Medical CenterBudget Analyst - Comprehensive Integrated Research OperationsKansas City, MO$60,800–$91,200 / yearSupport grant opportunities, facilitate proposal development, contribute to non-technical components of proposals, process proposals, develop budgets, support contract development, and ensure compliance with laws, regulations, policies, and terms and conditions. Job Description: Job Duties: • Manage and perform activities related to multiple areas of sponsored projects administration, including but not limited to pre-award and post-award activities for multiple cost centers.
Clinical 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.
Medical Research Associate ICON PlcMedical Research AssociateLenexa, KSAs a Medical Research Associate at ICON, you will be responsible for meeting/greeting clinical research volunteers as they come into the clinic, checking their vitals (height, weight, blood pressure, BMI), and essentially making sure the study participants are healthy eNugh to participate in the clinical trial according the protocol of a study. Preferred Background: Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician backgrounds are highly desired.
Medical Research Associate (Phlebotomist) - (PRN) ICON PlcMedical Research Associate (Phlebotomist) - (PRN)Lenexa, KSAs a Medical Research Associate at ICON, you will be responsible for meeting/greeting clinical research volunteers as they come into the clinic, checking their vitals (height, weight, blood pressure, BMI), and essentially making sure the study participants are healthy enough to participate in the clinical trial according the protocol of a study. Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.
Clinical Research Coordinator (Breast Cancer Prevention) Cancer Center University of Kansas Medical CenterClinical Research Coordinator (Breast Cancer Prevention) Cancer CenterWestwood East, KS$60,800–$91,200 / yearJob Description Summary: Job Description: The 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. Assist with study specific excel spread-sheet type protocol eligibility, demographics, evaluability and biomarker results summary to assist PI in monitoring study progression as well as gathering data for interim PMRC assessments and/ or presentations.
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.
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 Coordinator - Internal Medicine (Nephrology) University of Kansas Medical CenterClinical Research Coordinator - Internal Medicine (Nephrology)Kansas City, MO$60,800–$91,200 / yearJob Description Summary: The Clinical Research Coordinator in the Department of Internal Medicine, Division of Nephrology works collaboratively with multidisciplinary teams, research, and hospital staff to recruit, screen, educate, and assist in the kidney transplant clinical research studies. Additionally, the Clinical Research Coordinator monitors participant progress, documents and reports adverse events, and participates in periodic quality assurance audits of study protocols.
Graduate Research Assistant Kansas City UniversityGraduate Research AssistantKansas City, KansasOur annual campus security report lists campus crimes and statistics for the campus and public areas around campus for the last three years, in accordance with the Jeanne Clery Disclosure of Campus Security Policy and Campus Crime Statistics Act. Job Type: Student (Fixed Term)Job Description: The Graduate Research Assistant will help to recruit babies and conduct research appointments with babies and parents.
NewClinical Research Coordinator - Must be local to Overland Park, KS! EyeCare Partners LLCClinical Research Coordinator - Must be local to Overland Park, KS!Overland Park, KSSUMMARY: To provide clinical research support for studies involving human subjects including administration; project implementation, meeting support, quality assurance, and dissemination of results, recruitment; collection, recording, and editing of interview, questionnaire, and clinical data; performing quality assurance monitoring of study data; randomization of study participants; conducting case management tasks; scheduling participant appointments; supporting clinical and group intervention; review medical records following study protocols; and performing other duties in support of clinical trials services as assigned. Provide assistance in the administrative, technical and scientific day-to-day operation of the study to assure project goals and timelines are met, quality data is collected and managed, and to assure participant and/or data confidentiality.
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).
Study Start-Up Clinical Research Associate, Sponsor Dedicated IQVIAStudy Start-Up Clinical Research Associate, Sponsor DedicatedOverland Park, KansasThe Study Start-Up CRA is accountable for site selections as well as study-specific start-up activities and deliverables of assigned sites for Phase I-IV trials in the country in accordance with monitoring procedures and processes following ICH/GCP, local regulations and SOPs. Collaborates with the SSO Study Start-Up Manager, the SSO Study Start-Up Team Lead and global study team to ensure Study Start-Up timelines and deliverables are met according to country commitments .
Research Assistant - Radiology University of Kansas Medical CenterResearch Assistant - RadiologyKansas City, MO$22.88–$33.17 / hourPerform preprocessing and pipelining of functional and structural MRI and DTI data; prepare and analyze data for presentation; work at the command-line in for neuroimaging processing and analysis (FSL, AFNI, in-house software tools). Responsibilities include supporting MRI data acquisition workflows, performing image and data processing, and assisting with analysis procedures according to established study protocols.
Research Assistant - Surgery General University of Kansas Medical CenterResearch Assistant - Surgery GeneralKansas City, MO$22.88–$33.17 / hourThis position provides hands-on experience in pancreatic cancer while working closely with faculty and research team members to ensure adherence to study protocols and the accuracy of research data. Job Description Summary: This position will work closely with Dr. Dhawan and the other researchers in her lab at KU Medical Center (KUMC) to assist in the successful development and completion of basic science research studies in pancreatic cancer.
Clinical Research Engagement Lead (CREL) - Central Region (Kansas City, MO) Genentech IncClinical Research Engagement Lead (CREL) - Central Region (Kansas City, MO)Kansas City, MO$103,300–$191,900 / yearRelationship Management & Site Support: Builds deep, multi-stakeholder relationships at strategic sites (including investigators, pharmacists, and administration), acting as a "site champion" and Primary Point of Contact to maintain cross-study consistency and address site needs. Cross-Functional Collaboration & Reporting: Partners seamlessly with internal teams (e.g., Medical Affairs, Study Start-Up) and CROs to ensure unified site communication, while maintaining meticulous documentation of site visits and interactions in central systems (e.g., Veeva).
Clinical Research Nurse Coordinator University of Kansas Medical CenterClinical Research Nurse CoordinatorKS$70,200–$105,300 / yearThe position provides professional nursing care and patient monitoring for clinical trials and works collaboratively with multidisciplinary teams, research personnel, and hospital staff to recruit, screen, educate, and support participants throughout the clinical study coordination process. Job Description Summary: The Clinical Research Nurse Coordinator in the Cancer Center manages clinical research studies by coordinating and participating in a variety of complex activities involved in the collection, compilation, documentation, and analysis of clinical research data.
Clinical Research Coordinator - Cancer Center University of Kansas Medical CenterClinical Research Coordinator - Cancer CenterKS$60,800–$91,200 / yearJob Description Summary: The 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. 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 II ICON PlcClinical Research Associate IIKansas City, MOAs a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.
Research Assistant - Neurology University of Kansas Medical CenterResearch Assistant - NeurologyKansas City, MO$22.88–$33.17 / hourConfer with principal investigator to review work assignments and develop plans for research experiments and make minor modifications to existing laboratory procedures and techniques to meet the needs of the particular equipment as required. Job Description Summary: Perform a variety of duties involved in conducting physical, chemical, biological and other research laboratory tests, experiments and determinations to obtain data for research purposes.
Clinical Research Associate, Sponsor Dedicated IQVIA Holdings IncClinical Research Associate, Sponsor DedicatedOverland Park, KSEnsure 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, KSEnsure 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, Oncology or Immunology IQVIA Holdings IncClinical Research Associate, Sponsor Dedicated, Oncology or ImmunologyOverland Park, KS$69,800–$226,800 / yearJoin our team as a Clinical Research Site Manager, where you'll play a crucial role in ensuring our study sites operate seamlessly and adhere to all protocols, regulations, and sponsor requirements. Documentation: Ensure all site documents are filed in the Trial Master File (TMF) and Investigator's Site File (ISF) according to GCP/ICH and local regulations.
Clinical Research Associate, Full Service IQVIA Holdings IncClinical Research Associate, Full ServiceOverland Park, KS$47,400–$169,300 / yearEnsure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigators 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.