Senior Clinical Research Regulatory Manager
Saint Louis University
Saint Louis University seeks a Clinical Research Regulatory Manager to oversee regulatory activities for industry-sponsored and NIH-funded studies. You will coordinate IRB submissions, ensure FDA/GCP compliance, and support budgeting, contracts, and registry oversight across multiple units. The role requires strong knowledge of FDA regulations, human subjects protections, and Good Clinical Practice, with experience in regulatory workflows, training, and collaboration with investigators and #J-18808-Ljbffr Saint Louis University
- Washington University in St. Louis is seeking a Clinical Research Coordinator to oversee and coordinate complex clinical studies, ensure regulatory compliance, and support budget and billing processes. The role may supervise staff and serves as a resource to research teams...Senior
- ...NeuroGenomics and Informatics Center is hiring a Senior Clinical Research Coordinator. This person will oversee... ...smooth clinical operations, prepare regulatory compliance documents, coordinate... ...or conclusions of the same. Manages protocol study start up and study launch...SeniorWork experience placementWork at office
- ...University in St. Louis is seeking a nurse coordinator to lead a research project, coordinating enrollment of study subjects and... ...research integrity. Responsibilities include start-up activities, regulatory submissions, data collection, and coordinating specimen handling...Senior
- ...Madrid, Spain, is recognized for world‑class academics, life‑changing research, compassionate health care, and a strong commitment to faith and service. JOB SUMMARY The Clinical Research Regulatory Manager oversees clinical research regulatory activities across all units...SuggestedContract workWork at office
- ...Research CoordinatorLocation: ST. LOUIS, MO 63110Scheduled Hours... ...projects, data collection, and the management of data generated by study... ...to sponsor(s), IRB and regulatory agencies in accordance with... ...job posting.Work Experience: Clinical Research (1 Year)Skills: Clinical...SuggestedWork experience placementWork at office
$54.6k - $81.9k
...coordinator is responsible for managing all phases of study protocol... ...: Works closely with Senior Coordinator for management of... ...Establishes excellent rapport with research participants, staff, and... ...Cross Work Experience: Clinical Research (2 Years) Skills:...Full timeFor contractorsWork experience placementWork at office- Stifel is seeking a Compliance Assistant Manager-Advisory Services to oversee the advisory compliance program. You will lead and mentor analysts, drive process improvements, and ensure adherence to SEC/FINRA requirements. The role requires strong knowledge of the Investment...Senior
- Stifel, Incorporated is seeking a Compliance Assistant Manager‑Advisory Services to oversee daily administration of the advisory compliance program, mentor staff, and manage cross‑functional initiatives. You will ensure adherence to SEC/FINRA rules and firm policies while...Senior
$58.3k - $90.4k
...and coordinates complex or multi-site clinical research studies; serves as a resource to provide... ...a smooth operation, preparation of regulatory compliance and interaction with other... ...Description Primary Duties & Responsibilities Manages protocol study start up and study...Work experience placementWork at office- Washington University in St. Louis is seeking a Clinical Research Coordinator to support a complex study, coordinating with investigators, the sponsor, and participants, and overseeing protocol compliance. The role involves developing study materials, data collection, adverse...
$54.6k - $81.9k
...investigators as coordinator of a complex clinical research study; may be responsible for multiple... ...community and the study participants; manages and records all phases of study... ...protocol guidelines and requirements of regulatory agencies; establishes record-keeping systems...Work experience placementWork at office- ...seeks a coordinator in the THuNDR Laboratory for postmortem brain research and coordination across AD and movement disorder studies. You... ...collection, and preparing progress reports and manuscripts; this is a non-clinical #J-18808-Ljbffr Washington University in St. Louis
- Washington University in St. Louis is seeking a Clinical Research Coordinator to screen and enroll patients in trials, coordinating collection... ...of clinical research experience; duties include protocol management, data collection, adverse event reporting, and collaboration...
- ...seeks a highly organized coordinator to refer and track research participant study visits for the Memory and Aging Project... ...as a coordinator of a basic to moderately complex clinical research study; may manage multiple studies, acting as a liaison with the school, sponsor...
- ...coordinator to refer and track research participant study visits for... ...basic to moderately complex clinical research study; may be responsible... ...:Implements and manages all phases of study/protocol;... ...guidelines and requirements of regulatory agencies; establishes record-...For contractorsWork experience placementWork at office
- ...University in St. Louis is seeking a Research Coordinator to support the... ...with regular desk work and clinical duties. Primary duties... ...coordinating all study phases, ensuring regulatory compliance, enrolling... ...obtaining informed consent, and managing data and reports. #J-18808-...
- Washington University in St. Louis is seeking a Clinical Research Coordinator for the Radiology Clinical Research Core (RadCore). The role... ...studies, handling patient recruitment, data collection, and regulatory compliance in a hybrid, Monday-Friday schedule. Responsibilities...Monday to Friday
- ...SummaryThis position will be in the Radiology Clinical Research Core (RadCore). RadCore supports novel... ...entry, patient education, ensuring regulatory compliance, and maintaining accurate... ...of new studies.Implements and manages all phases of study/protocol; ensures...For contractorsWork experience placementWork at officeMonday to FridayFlexible hours
- Clinical Research Coordinator II Our clinical research company is looking to hire a qualified candidate for the full-time position of Clinical... ...Possess an acute attention to detail for clean data entry, regulatory compliance, productive site visits, efficient study set-up...Full timeTemporary workWork visaFlexible hours
- Overview Velocity Clinical Research is an owned and integrated research site organization, providing... ...Research Coordinator II conducts and manages multiple clinical trials from start up... ..., protocol training,collection of regulatory documents, conducting visits, ensuring...Work at officeFlexible hours
$23.63 - $35.49 per hour
Washington University in St. Louis is seeking a Clinical Research Coordinator I to assist in managing clinical research studies. Responsibilities include recruiting participants, ensuring protocol compliance, and analyzing data. Ideal candidates should have a Bachelor's...Hourly payFull time- Washington University in St. Louis is seeking a Clinical Research Coordinator to screen and enroll patients for trials, coordinate collection... ...the clinical teams through protocol follow-up. The CRC will manage multiple studies when needed and ensure patient safety and ethical...
- Velocity Clinical Research, Inc. is seeking a Clinical Research Coordinator II to manage multiple trials from start-up to close-out in compliance with protocol, GCP, and... ...data accuracy, patient safety, and timely regulatory/documentation tasks. You will coordinate recruitment...
$56.2k - $96.1k
...of stable-isotope labeled peptides to clinical translational studies in diagnostic and... ...Study to Understand Novel Biomarkers in Researching Dementia (SUNBIRD) to validate blood biomarkers... .../projects, data collection, and the management of data generated by study protocols....Work experience placementWork at office- ...in St. Louis is seeking an RN Research Nurse Coordinator I to support the Center for Clinical Studies. You will coordinate... ...participants, and ensure protocol and regulatory compliance while safeguarding... ...teams, educate staff, manage source documents, and help maintain...
- Saint Louis University seeks a Clinical Research Regulatory Manager to oversee regulatory activities for industry-sponsored, NIH, and grant-funded studies. The role coordinates IRB submissions, maintains compliance with FDA regulations, and supports clinical trial oversight...Senior
- Position Summary The Clinical Research Coordinator (CRC) screens and enrolls patients to trials... ...and Principal Investigator (PI) in managing the clinical and patient study requirements... ...guidelines and requirements of regulatory agencies; establishes record-keeping systems...Work experience placement
$47.4k - $71.2k
Position Summary The Clinical Research Coordinator (CRC) screens and enrolls patients to trials... ...and Principal Investigator (PI) in managing the clinical and patient study requirements... ...guidelines and requirements of regulatory agencies; establishes record‑keeping systems...Work experience placementWork at office$54.6k - $81.9k
...investigators as a data coordinator of numerous clinical research trials of all complexities, extracting... ...and Principal Investigator (PI) manage and record data for all phases of study... ...guidelines and requirements of regulatory agencies; establishes record-keeping systems...For contractorsWork experience placementWork at office- Washington University in St. Louis seeks a Clinical Research Coordinator III to oversee complex clinical studies, coordinate multi-site operations, and ensure regulatory compliance. The role includes guiding staff, preparing regulatory documents, and liaising with PI and...Senior
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