Clinical Research Coordinator - Women''''s Health Department University Health.Clinical Research Coordinator - Women''''s Health DepartmentKansas City, MOYou'll use your clinical knowledge, organizational skills, sound judgment, and attention to detail to ensure studies are conducted safely, efficiently, ethically, and in accordance with research protocols, Good Clinical Practice (GCP), federal and state regulations, and institutional requirements. Maintain complete, accurate, and audit-ready study records, including regulatory documents, informed consent and privacy authorization forms, IRB approvals, source documentation, investigational product records, delegation logs, case report forms, and study correspondence.
Clinical Research Coordinator - Women's Health Department Truman Medical CentersClinical Research Coordinator - Women's Health DepartmentKansas City, MOYou'll use your clinical knowledge, organizational skills, sound judgment, and attention to detail to ensure studies are conducted safely, efficiently, ethically, and in accordance with research protocols, Good Clinical Practice (GCP), federal and state regulations, and institutional requirements. Maintain complete, accurate, and audit-ready study records, including regulatory documents, informed consent and privacy authorization forms, IRB approvals, source documentation, investigational product records, delegation logs, case report forms, and study correspondence.
Onsite Clinical Research Coordinator - Mercy STL - Full Time MercyOnsite Clinical Research Coordinator - Mercy STL - Full TimeSaint Louis, MOThe Clinical Research Coordinator is responsible for the day-to-day operational tasks related to clinical trials and performs a variety of duties including, but not limited to: volunteer recruitment, drug/device/supply inventory maintenance, interaction with physicians, nurses, office staff, patients, and clinical monitors. This role manages the day-to-day operations of clinical trials, including patient recruitment, study coordination, data collection, regulatory compliance, and communication with sponsors, physicians, patients, and research staff.
Clinical Research Nurse - Mercy Springfield MercyClinical Research Nurse - Mercy SpringfieldSpringfield, MissouriThe Clinical Research Nurse is responsible for the day-to-day operational tasks related to clinical trials and performs a variety of duties including, but not limited to, volunteer recruitment, drug/device/supply inventory maintenance, interaction with physicians, nurses, office staff, patients, and clinical monitors. From day one, Mercy offers outstanding benefits - including medical, dental, and vision coverage, paid time off, tuition support, and matched retirement plans for team members working 32+ hours per pay period.
Clinical Research Nurse - Mercy South - Full Time MercyClinical Research Nurse - Mercy South - Full TimeSaint Louis, MOThe Clinical Research Nurse is responsible for the day-to-day operational tasks related to clinical trials and performs a variety of duties including, but not limited to, volunteer recruitment, drug/device/supply inventory maintenance, interaction with physicians, nurses, office staff, patients, and clinical monitors. From day one, Mercy offers outstanding benefits - including medical, dental, and vision coverage, paid time off, tuition support, and matched retirement plans for team members working 32+ hours per pay period.
Remote LTC Pharmacy Data Entry Technician SymbriaRemote LTC Pharmacy Data Entry TechnicianSt. Louis, MissouriRemoteFull timeFor more than 20 years, Symbria has been providing an outstanding work environment for talented employees to deliver patient-centered care to the geriatric population in senior-living and post-acute settings. For more than 20 years, Symbria has been providing an outstanding work environment for talented employees to deliver patient-centered care to the geriatric population in senior-living and post-acute settings.
Clinical Research Coordinator II Velocity Clinical Research, Inc.Clinical Research Coordinator IISt. Louis, MissouriTemporaryImplement and coordinate assigned clinical trials including start up, vendor management,subject recruitment, source development review, scheduling subjects, protocol training,collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports. Overview: Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites.
NewNETWORK ENGINEER-ENTRY #00061761 University of MissouriNETWORK ENGINEER-ENTRY #00061761Rolla, MO$55,000–$69,576 / yearThe On-site Network Engineer-Entry, under general direction, performs routine network engineering functions, such as troubleshooting, analysis, research, problem solving, and maintenance of a distributed network. Administer and maintain LAN, WAN, and Data Center operations and equipment to ensure maximum availability of the high-quality network resources currently provided to the campus community.
NewClinical Research Nurse Hannibal Regional HospitalClinical Research NurseHannibal, MOCurrent licensure in the State of Missouri as a Registered Nurse is required, or ability to obtain Experience in Microsoft Word, Excel, and Outlook required Experience in phlebotomy required Experience placing IVs and giving infusions required Experience in clinical research preferred Highly effective verbal and written communication skills Ability to assess laboratory results and trends to escalate clinically significant lab values to the Principal Investigator Ability to demonstrate knowledge and skills necessary to provide care appropriate to the population and indication being studied Ability to follow detailed and specific timelines for dosing, blood draws, and other assessments BLS Certification required. Responsibilities include participant screening and enrollment, informed consent, clinical assessments, administration of Investigational Product and other protocol-required treatments, specimen collection, monitoring of participant safety, identification and management of adverse events, patient education, and accurate documentation of clinical research activities.
Clinical Research Study Assistant II (Hybrid) - Pediatrics Hematology & Oncology Washington University in St LouisClinical Research Study Assistant II (Hybrid) - Pediatrics Hematology & OncologySt. Louis, MORemote$19.93–$29.93 / hourAssists investigators with moderately complex clinical research and social science research studies by assisting with enrollments, data, and research compliance needs related to Pediatric Hematology/Oncology and vascular anomalies clinical research. The screenings will include criminal background check and, as applicable for the position, other background checks, drug screen, an employment and education or licensure/certification verification, physical examination, certain vaccinations and/or governmental registry checks.
NewPart-time Project Coordinator (Research Assistant) - Data Systems and Evaluation, UMKC School of Nursing and Health Studies University of MissouriPart-time Project Coordinator (Research Assistant) - Data Systems and Evaluation, UMKC School of Nursing and Health StudiesKansas City, MOThe 12-month, part time (70% FTE - 28 hours per week) Project Coordinator (Research Assistant) - Data Systems and Evaluation position will support the implementation of a federally funded, national multi-site evaluation conducted by the University of Missouri-Kansas City in partnership with the Health Resources and Services Administration HIV/AIDS Bureau (HRSA HAB). The Project Coordinator will play a central role in developing and maintaining the project's evaluation infrastructure, coordinating data collection and submission processes, monitoring data quality, supporting qualitative research activities, and assisting implementation sites with evaluation systems and reporting requirements.
NewResearch Assistant Howard UniversityResearch AssistantColumbia, MO$20–$29 / hourConducting research that specifically addresses the healthcare needs of minority populations aiming to enhance the quality of life and social-economic status of minority communities through improved healthcare interventions. The tasks include performing imaging experiments for studies ranging from preclinical to translational research, analyzing research data, and writing research reports.
Clinical Research Study Assistant II - Medical Oncology Washington University in St LouisClinical Research Study Assistant II - Medical OncologySt. Louis, MO$19.93–$29.93 / hourCollects data from study participants, medical records, interviews, questionnaires, diagnostic tests and other sources; performs basic evaluation and interpretation of collected data and prepares appropriate reports and documentation as necessary; prepares and distributes study packets and information. Performs basic/scripted assessments to confirm eligibility to participate in study; explains and schedules laboratory and diagnostic procedures and/or treatment as required in the study; refers participants to basic resources as necessary.
Clinical Research Study Assistant II - Emergency Medicine Washington University in St LouisClinical Research Study Assistant II - Emergency MedicineSt. Louis, MO$19.93–$29.93 / hourCollects data from study participants, medical records, interviews, questionnaires, diagnostic tests and other sources; performs basic evaluation and interpretation of collected data and prepares appropriate reports and documentation as necessary; prepares and distributes study packets and information. Performs basic/scripted assessments to confirm eligibility to participate in study; explains and schedules laboratory and diagnostic procedures and/or treatment as required in the study; refers participants to basic resources as necessary.
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.
Specialized Tax Services - Research & Development Tax - Senior Manager PricewaterhouseCoopers LLPSpecialized Tax Services - Research & Development Tax - Senior ManagerSt. Louis, MO$124,000–$335,000 / yearAs a Specialized Tax Services - Research & Development Tax - Senior Manager, you will focus on providing tax advice and solutions to clients in complex and niche areas of taxation, including accounting methods, fixed-assets, and research and development tax credits. PwC does not intend to hire experienced or entry level job seekers who will need, now or in the future, PwC sponsorship through the H-1B lottery, except as set forth within the following policy: https://pwc.to/H-1B-Lottery-Policy .
Specialized Tax Services - Research & Development Tax - Senior Associate PricewaterhouseCoopers LLPSpecialized Tax Services - Research & Development Tax - Senior AssociateSt. Louis, MO$77,000–$214,000 / yearAs a Specialized Tax Services - Research & Development Tax - Senior Associate, you will focus on providing tax advice and solutions to clients in complex and niche areas of taxation, such as accounting methods, fixed-assets, and research and development tax credits. PwC does not intend to hire experienced or entry level job seekers who will need, now or in the future, PwC sponsorship through the H-1B lottery, except as set forth within the following policy: https://pwc.to/H-1B-Lottery-Policy .
Specialized Tax Services - Research & Development Tax - Manager PwCSpecialized Tax Services - Research & Development Tax - ManagerSaint Louis, MO$99,000–$266,000 / yearAs a Specialized Tax Services- Research & Development Tax- Manager, you will provide tax advice and solutions to clients in complex and niche areas of taxation, including accounting methods, fixed-assets, and research and development tax credits. PwC does not intend to hire experienced or entry level job seekers who will need, now or in the future, PwC sponsorship through the H-1B lottery, except as set forth within the following policy: https://pwc.to/H-1B-Lottery-Policy .
PRN Research Coordinator - Emergency Medicine University Health.PRN Research Coordinator - Emergency MedicineKansas City, MOMaintain accurate and complete study documentation, including regulatory files, informed consent and privacy authorization forms, IRB approvals, source documentation, case report forms, study communications, and drug or test article accountability records. As a Clinical Research Coordinator I, you'll play an important role in bringing clinical research studies to life-from study start-up and participant recruitment through study completion.
PRN Research Coordinator - Emergency Medicine Truman Medical CentersPRN Research Coordinator - Emergency MedicineKansas City, MOMaintain accurate and complete study documentation, including regulatory files, informed consent and privacy authorization forms, IRB approvals, source documentation, case report forms, study communications, and drug or test article accountability records. As a Clinical Research Coordinator I, you'll play an important role in bringing clinical research studies to life-from study start-up and participant recruitment through study completion.