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.
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) ICON PlcMedical Research Associate (Phlebotomist)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 to 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.
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.
Research Associate Pilot Lab Kemin Industries IncResearch Associate Pilot LabLenexa, KSWe create solutions that strengthen health and wellbeing, provide nutrition and immune support for pets and production animals, safeguard the planet's natural resources, and protect the global food supply chain for generations to come. We employ 3,500 global employees and operations in 90 countries, including manufacturing facilities in Belgium, Brazil, China, Egypt, India, Italy, San Marino, Singapore, South Africa, and the United States.
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.
Research Associate Kansas City UniversityResearch AssociateKansas City, MOOur 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. Proven ability to manage research projects and coordinate with multiple stakeholders, including training and overseeing student researchers and junior research staff.
Senior Medical Research Associate (EMT) ICON PlcSenior Medical Research Associate (EMT)Lenexa, KSThis role blends hands-on patient care with research responsibilities and is ideal for someone who thrives in a fast-paced environment, is confident in emergency response, and can ensure high-quality and compliant study execution. Perform EMT-level procedures within certification scope, including blood draws, specimen collection, wound care, and stabilization during urgent or unexpected clinical situations.
Senior Medical Research Associate ICON PlcSenior Medical Research AssociateLenexa, KSWhether you're exploring a career in clinical research or already have experience in the field, this role offers a chance to contribute to work that supports the future of healthcare and disease management. Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.
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 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.
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 .
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.
Animal Health Clinical Research Associate III Argenta LtdAnimal Health Clinical Research Associate IIIShawnee, KSOur Clinical Research Associates add value through the following responsibilities: Coordinates and conducts GCP and study protocol training at study sites and assures training is documented Builds rapport with study site staff to assure compliance with the protocol, applicable regulatory and guidance documents, SOPs, and all study activities Assists in reviewing the study records and all study notebooks to ensure contents are current and complete Assists in providing tracking and Quality Control (QC) of data as required and assists with responses to QA audits Evaluates Investigators and assists with selection of appropriate sites to conduct clinical studies Collaborates with the study Project Manager to assure study sites selected meet the needs of the study protocol Monitors assigned study sites through review of electronic data capture (EDC) systems, faxed, emailed, and paper documentation. Serves as the liaison between Argenta US Clinical and study site personnel Facilitates clarifications, corrections, and data query resolution with study sites or data management personnel Tracks adverse events (AE's) encountered in clinical studies and ensures all serious AEs and non-serious AEs are documented and communicated appropriately to the Project Manager and Sponsor Learns to assist with facilitates clarifications, corrections, and data query resolution with study sites or data management personnel.
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.
Senior Clinical Research Associate ICON PlcSenior Clinical Research AssociateLenexa, KSRemoteFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. 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, 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 / yearp>Join 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.
Clinical Research Associate II, Phase I Fortrea IncClinical Research Associate II, Phase IRemote Kansas, KSRemote$105,000–$118,000 / 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.
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.
Senior Clinical Research Associate IRESenior Clinical Research AssociateKansas City, MissouriThe ideal candidate will have cardiovascular medical device monitoring experience- however, cardiovascular/electrophysiology pharma monitoring 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.
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Associate Dean of Research - SON University of Kansas Medical CenterAssociate Dean of Research - SONKansas City, MOli>Ensure appropriate research administration, faculty and staff effort aligns appropriately with research funding and institutional expectations, integrity of research data and associated electronic databases and safeguarding research‑related physical assets and property. If selected as a final candidate for this position, you may be required to complete the Association of American of Universities Representations and Warranties document and sign a release of records that will allow the University of Kansas Medical Center to conduct a further background check with former employers.
Research Scientist or Senior Research Scientist, Dept of Ophthalmology, School of Medicine University of MissouriResearch Scientist or Senior Research Scientist, Dept of Ophthalmology, School of MedicineKansas City, MOUMKC provides unique opportunities for research and health care collaboration across its Schools of: Medicine, Dentistry, Nursing & 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. The Vision Research Center (VRC) at UMKC is the Department of Ophthalmology's research arm, providing residents and fellows with comprehensive research opportunities, including basic research, translational research and clinical trials.
Research Scientist or Senior Research Scientist, Dept of Ophthalmology, School of Medicine University of Missouri-Kansas CityResearch Scientist or Senior Research Scientist, Dept of Ophthalmology, School of MedicineKansas City, MOUMKC provides unique opportunities for research and health care collaboration across its Schools of: Medicine, Dentistry, Nursing & Health Studies, and Pharmacy as well as University Health Physicians, regional health care institutions, and the University of Missouri Systems NextGen Data Science and Analytics Innovation Center. The Vision Research Center (VRC) at UMKC is the Department of Ophthalmology's research arm, providing residents and fellows with comprehensive research opportunities, including basic research, translational research and clinical trials.
Research Scientist- Remote Community Health Center IncResearch Scientist- RemoteKSRemoteThe system delivers primary care to more than 150,000 patients in Connecticut, and extends access to specialty care for more than 2.5 million individuals across the U.S. It is a national accrediting body for organizations training advanced practice providers, and offers accredited education and training for Medical Assistants in multiple states. As an incubator for new ideas in areas including social justice, the environment, and social determinants of health, the MWHS is addressing challenges faced by providers caring for underserved communities, creating innovative and impactful initiatives led by nationally and internationally recognized experts.
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.
Research Technician I Eurofins Scientific SEResearch Technician ILenexa, KSEurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing. Basic Minimum Qualifications: Bachelor''s degree in chemistry, biology, biochemistry, or other related degree concentration, or equivalent directly-related experience (At least six months related experience from internship, independent research, or industry laboratory.
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.
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 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.
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 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.
NewNeonatal Research Faculty (MD, PhD, or MD/PhD) Children's Mercy Hospital (MO)Neonatal Research Faculty (MD, PhD, or MD/PhD)Kansas City, MOThe Division of Neonatology (Director: Dr. Steve Olsen) and the Neonatal Diseases Research Program (Director: Dr. Venkatesh Sampath), along with the Childrens Mercy Research Institute (CMRI Director: Dr. Tom Curran) announce a national search for an MD, PhD, or MD/PhD scientist to conduct translational or basic science research in the areas of neonatal lung or gut injury. Active collaborations with the Childrens Mercy Center for Pediatric Genomic Medicine (Director: Dr. Tomi Pastinen) are underway for advanced sequencing-based discovery of human genetic loci affecting several neonatal diseases and include the use of single-cell sequencing to characterize cellular phenotypic alterations in pre-clinical models.
Part-Time Office Support Assistant, UMKC Undergraduate Research University of MissouriPart-Time Office Support Assistant, UMKC Undergraduate ResearchKansas City, MOSenior Student Service Coordinator - Writing Center Tutoring Coordinator. Business Support Specialist Sr, Civil and Environmental Engineering.
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.
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 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;].
Director Plant Operations Research Medical Center Full Time Days No Weekends Compu-Vision Consulting Inc.Director Plant Operations Research Medical Center Full Time Days No WeekendsKansas City, MOThe Director of Facilities, reporting to the COO/Associate Administrator, manages and maintains buildings, grounds, utilities, and non-clinical equipment for Research Medical Center, Research Medical Center Brookside, Research Psychiatric and Belton Regional Medical Center campus. Strong leadership experience, tenured work history (not interested in candidates who does not stay long in their previous roles), strongly prefer someone who has experience working with hospital metrics.
Research Technician - ONC Radiation Oncology University of Kansas Medical CenterResearch Technician - ONC Radiation OncologyKansas City, MO$21.06–$27.40 / hourJob Description Summary: The Research Technician will be involved in performing routine laboratory techniques, inventory, and animal colony maintenance in Dr. Gregory Gan research lab. 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 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;].
Senior Research Scientist ICON PlcSenior Research ScientistLenexa, KSWe also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being.
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.
Senior Grants and Contracts Administrator (Pre-Award), Office of Research and Innovation University of MissouriSenior Grants and Contracts Administrator (Pre-Award), Office of Research and InnovationKansas City, MO$53,973–$56,973 / yearAs part of your total compensation, the University offers a comprehensive benefits package, including medical, dental and vision plans, retirement, paid time off, short- and long-term disability, paid parental leave, paid caregiver leave, and educational fee discounts for all four UM System campuses. Salary is determined by a variety of factors, including but not limited to, the individual's particular combination of education, skills, and experience, as well as organizational requirements.
Grants and Contracts Administrator (Post-Award), Office of Research and Innovation University of MissouriGrants and Contracts Administrator (Post-Award), Office of Research and InnovationKansas City, MO$53,973.30–$56,013 / yearORI has responsibility for pre-award and award administration and is the institutional unit authorized by the Curators of the University of Missouri to submit proposals to and accept awards from external entities for financial support in the form of grants, contracts, and cooperative agreements. As part of your total compensation, the University offers a comprehensive benefits package, including medical, dental and vision plans, retirement, paid time off, short- and long-term disability, paid parental leave, paid caregiver leave, and educational fee discounts for all four UM System campuses.