Clinical Research Coordinator: Study Operations & Compliance
Cincinnati Children's Office of Academic Affairs and Career Development
Cincinnati Children’s is seeking a clinical research support professional to assist in coordinating studies, preparing regulatory documents, and ensuring IRB compliance. The role includes patient recruitment, data entry, and collaboration with the clinical team to advance translational pharmacology research. The position emphasizes adherence to GCP/ICH, proper documentation, and maintaining study records across multiple systems, with routine collaboration across departments. #J-18808-Ljbffr Cincinnati Children's Office of Academic Affairs and Career Development
- Cincinnati Children's is seeking Clinical Research Coordinators to support innovative clinical and translational... ...recruitment and enrollment, conduct study visits, manage regulatory... ...specimens, oversee study data, and ensure compliance with research protocols and regulatory...Suggested
- Cincinnati Children’s is seeking qualified Clinical Research Coordinators (CRCs) to support vivacious translational and clinical... ...participant recruitment, enrollment, and study visits, while ensuring regulatory compliance and accurate data handling across multiple studies...SuggestedWork at office
- ...staff member at the Burnet Campus. Primary responsibilities include coordinating studies, regulatory documentation, participant recruitment, communication with teams, and data management for clinical research projects. Qualifications include a high school diploma or...SuggestedFull timeWork at office
$24.46 - $27.73 per hour
...status. JOB RESPONSIBILITIES Study Conduct/ Clinical Research Practice - Assist in coordinating studies by preparing personnel... ...with the protocol, manual of operations, standard operating procedure... ...with equipment. Regulatory Compliance and Documentation - Identify...OperationsFull timeWork experience placementLocal areaShift workWeekend work$74.3k - $94.74k
...and Behavioral Pediatrics conducts clinical research focused on improving outcomes for... ...The Senior Clinical Research Coordinator will provide leadership for clinical research studies, overseeing study operations, regulatory compliance, participant engagement, data management...OperationsFull timeLocal areaShift workWeekend work- ...continuing to add established Clinical Trial Project Managers with a... ...for day-to-day operations of the project, as defined by... ...project-specific issues and study deliverablesMaintain in depth... ...supervision of project Clinical Research Associates and monitoring deliverablesQualificationsBachelor...OperationsContract workWork at officeWork from home
- ...continuing to add established Clinical Trial Managers and Project... ...accountability for day-to-day operations of the project, as defined by... ...project-specific issues and study deliverablesMaintain in depth... ...supervision of project Clinical Research Associates and monitoring...OperationsContract workWork at officeWork from home
- ...nation's leading provider of clinically integrated eye care. Our... ...Oversees details of studies. Ensures compliance with study review board and... ...study selection; correspond/coordinate with the sponsor/CRO; prepare... .../manage site for clinical research studies, create study-...Full timeInterim roleWork at officeFlexible hours
$120k - $135k
Clinical Project Manager - Oncology (Client... ...advancing cancer research and bringing innovative... ...of oncology studies across multiple... ...critical role in the operational leadership and... ...specialty providers Coordinate Clinical Trial... ...readiness and compliance with applicable regulations...OperationsRemote jobContract workWork at officeImmediate startWorldwideFlexible hours$24.46 - $27.73 per hour
...seeking a full-time Ophthalmology staff member at the Burnet Campus. This role supports clinical research activities within the Ophthalmology department, including protocol coordination, consent processes, and data management. Starting pay is available, with range $24.46-...Hourly payFull time- Senior Clinical Project Manager - up to $15... ...management of daily trial operations. Often functions... ...oversight and coordination across functional... ...contact, leading study meetings,... ...performance, and compliance with project and... ...years of clinical research experience at a CRO...OperationsRemote jobFull timeContract workWork experience placementWork from homeRelocation package
- Clinical Project Manager III/ Senior (level... ...management of daily trial operations. Often functions... ...oversight and coordination of the... ...projects to ensure compliance with International... ...oversight of Clinical Research Associate (CRA)... ...TMF for assigned studies ensuring that all...OperationsFull timeContract workWork experience placementRemote workWork from homeRelocation package
- ...impact medicines through clinical development with a... ...management, clinical operations, project management, vendor oversight, research, protocol development,... ...to identify risks to study/project quality, budget... ...in the development and coordination of regulatory documents...OperationsFull timeWork at office
- ...Clinical Research Coordinator IIThe Clinical Research Coordinator II conducts and manages multiple clinical trials from start up through study close out in accordance with the study protocol, GCP, and Velocity's SOPs.ResponsibilitiesDuties/Responsibilities:Conduct and...Work at officeFlexible hours
- ...Clinical Research CoordinatorTriHealth offers Clinical Research Coordinators a purpose-driven career coordinating Phase II–IV clinical... ...subject assessment, regulatory compliance, and protocol execution,... ...all IRB/FDA requirements in study submission.Assesses potential...Full timeShift work
$56.78k - $62.15k
...vary based on FTE status. Join Our Clinical Research Coordinator Talent Community Cincinnati... ...recruitment and enrollment, conduct study visits, manage regulatory documentation... ...multidisciplinary teams, and ensure compliance with research protocols and regulatory...Full timeWork experience placementWork at officeShift workWeekend work- ...The Site Relationship Coordinator is a new role within the Clinical Monitoring team at Medpace... ...exciting career in the research of drug and medical device... .../alignment with studies and/or therapeutic areas... ...clinical trial management and operational procedures, including GCP...Full timeContract workWork at officeWork from home
- ...TriHealth offers Clinical Research Coordinators a purpose-driven career coordinating... ...assessment, regulatory compliance, and protocol execution, along... ...for site selection, study preparation and execution... .... Adheres to the standard operating procedures of the TriHealth...Full timeReliefShift workDay shift
- Velocity Clinical Research, Inc. is seeking a Clinical Research Coordinator II to oversee multiple trials from initiation to close-out in accordance with study protocols, GCP, and Velocity SOPs. Responsibilities include start-up coordination, subject recruitment, data...Work at office
- Coordinate the conduct of Phase I through Phase IV clinical research studies in accordance with Good Clinical Practices (GCPs), International... ...Guideline and Standard Operating Procedures (SOPs) beginning... ...procedures are conducted in compliance with the clinical protocol;...Local areaWork from home
- CTI Clinical Trial and Consulting Services in Cincinnati seeks a Clinical Research Coordinator to coordinate Phase I through IV studies in line with GCPs, ICH guidelines, and SOPs, from pre-study... ...templates, and ensure protocol compliance while maintaining participant...
- ...seeking a full-time, office-based Project Coordinator to join our Clinical Trial Management team. This position... ...work environment in clinical research and want to develop your career even... ...status reports;Interact with the Sponsor, study sites, and internal associates;Provide...Full timeContract workWork at officeWork from home
- ...Hospital in Cincinnati, OH is seeking a Clinical Research Coordinator. The role oversees coordination of... ...focus on safety, integrity, and protocol compliance. The incumbent will educate, liaise with sponsors, and ensure timely study start-up, execution, and close-out per...
- Ctifacts is seeking a Clinical Research Coordinator for our Cincinnati, OH site. The role encompasses coordinating Phase I-IV studies following GCPs, SOPs, and regulatory standards. You... ...patient safety and protocol compliance. The ideal candidate has 1+ year CRC...
- ...headquartered in Cincinnati, seeks an entry-level Research Coordinator to develop a foundational understanding of clinical research under physician and scientist... ...collaborate with sponsors and vendors to support study execution in a dynamic, team-driven environment...
- ...Endocrine, and Metabolic research areas. This is an... ...from academia to the Clinical Trials Industry ! LOCATION... ...our global Clinical Operations team. The aCTM will be... ...closely with Project Coordinators and Clinical Trial Managers... ...collaborate on global study activities; working...OperationsFull timeContract workWork at officeWork from home
- Cincinnati Children's, Allergy Department, Burnet Campus, is seeking a Clinical Research Coordinator for a full-time day shift. This 40-hour FTE position supports complex multi-center studies under the PI, with collaboration across divisions to ensure compliant trial conduct...Full timeWork at officeDay shift
- Cincinnati Children's is seeking a Clinical Research Coordinator to support multi-center trials in the DDBP department. You will collaborate with... ...collection, and mentor staff to ensure protocol adherence and study quality. The role requires a Bachelor's degree in a...Full timeWork at officeDay shift
- Medpace Reference Laboratory is seeking a Project Coordinator to join their team in a fast paced, team... ...you can apply your life sciences background to clinical research and shipment logistics. You will manage study timelines, work with Biorepository, Project Management...
- ...OH is seeking an experienced Clinical Project Manager for a full-time... ...lead trial management, clinical operations, and vendor oversight across phases I-III, while coordinating protocol development and... ...Responsibilities include developing study plans, timelines, budgets,...OperationsFull time
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