Clinical Research Pro II — Trials Operations & Coordination
University of Cincinnati
A leading medical school in Cincinnati is hiring a Clinical Research Professional to support clinical trials within its Cancer Center. The role requires a Bachelor's degree and relevant experience, focusing on patient interaction and documentation. Responsibilities include consenting participants, coordinating medical procedures, and maintaining electronic records. The position offers competitive compensation and a robust benefits package emphasizing work-life balance and professional development opportunities. #J-18808-Ljbffr University of Cincinnati
- ...UC Cancer Center is seeking a Clinical Research Professional / Clinical Research Professional II to join its on-site team in Cincinnati... ...oncology clinical studies, coordinates participant activities, and... ...regulatory compliance across trials. Posting date 10/16/26 signals...Suggested
- Medpace, the Cincinnati-based global clinical research organization, seeks an Entry Feasibility Coordinator to join our clinical operations team. You will analyze data from internal and... ...enrollment planning for global clinical trials. You will coordinate feasibility...Operations
- Cincinnati Children's is seeking CRC II/III professionals to support study conduct in the Behavioral Med-Clin Psychology department. Responsibilities include coordinating protocols, consenting, and data management, with a focus on regulatory compliance and participant engagement...OperationsFull time
- ...seeking an Experienced Feasibility Coordinator, who will be a member of our global clinical operations team. By working cross... ...enrollment planning for global clinical trials. If you are an individual with... ...and expertise in clinical research and an interest in data analysis...OperationsContract workWork from home
- A major public research university is seeking a Clinical Research Professional to support their Cancer Program. The ideal candidate will coordinate clinical trials, manage patient appointments, and maintain accurate clinical documentation. A Bachelor's degree in a related...Suggested
- Cincinnati Children’s is seeking staff to support clinical research activities within Behavioral Med-Clin Psychology. The role supports... ...setting. Responsibilities include preparing IRB documents, coordinating participant visits, and ensuring data integrity in electronic...OperationsWork at office
- Cincinnati Children’s is seeking a dedicated clinical research support professional to assist with study coordination at the Burnet Campus in Cincinnati. The role involves preparing documents for IRB review, assembling lab kits, and ensuring proper sample handling and...
- Cincinnati Children’s is seeking an individual to support Clinical Research activities within the Behavioral Med-Clin Psychology department. The role involves coordinating studies, preparing protocols and consent documents, and ensuring regulatory compliance throughout...Work at office
$37.8k - $94.5k
...accelerate your career in clinical research? Join Avacare, a... ...where Clinical Research Coordinators (CRCs) gain... ...exposure to diverse trials, hands-on responsibilities... ...future roles in clinical operations, monitoring, and... ...with participants. CRC II: Minimum of 3 years as...OperationsFull timePart timeWork at officeLocal areaImmediate startWorldwide- Job SummaryOur clinical operations activities are growing rapidly, and we are currently seeking talent Clincial Research Coordinators to join our Study Start-up team. This position works both... ...and plays a key role in the clinical trial management and study start-up...OperationsContract workWork from home
- Job SummaryOur clinical operations activities are growing rapidly, and we... ...based Regulatory Submissions Coordinators to join our Study Start-up... ...a key role in the clinical trial management and study start-... ...ResponsibilitiesCommunicate with research sites (doctor's offices,...OperationsFull timeContract workWork at officeWork from home
$24.46 - $28.53 per hour
Cincinnati Children's is seeking a Clinical Research Coordinator II to support pediatric studies at the Burnet Campus. The role involves coordinating study activities, recruiting participants, and ensuring regulatory compliance in a team-based environment. Starting pay...Hourly payFull time- Velocity Clinical Research, Inc. is seeking a Clinical Research Coordinator I to conduct and manage clinical trials in accordance with study protocol, GCP, and Velocity SOPs. You will coordinate trials from start-up to close-out, supervise data entry, and ensure regulatory...
$37.8k - $94.5k
...Clinical Research Coordinator position at an SMO managing multiple clinical trials with exposure to diverse therapeutic areas. Role requires... ...on clinical skills and site operations knowledge, with... ...site (CRC I) or 3+ years (CRC II) ~ Proficiency obtaining vital...OperationsWork at office- ...Hospital Health Network is seeking a Clinical Research Medical Assistant to support daily clinical trial activities and patient flow in... ..., phlebotomy, data entry, and coordinating with study staff to ensure protocol compliance and smooth operations. A Medical Assistant...Operations
$56.78k - $63.96k
...Responsibilities Study Conduct/ Clinical Research Practice - Maintain... ...with the protocol, manual of operations, standard operating procedures... ...aspects of conducting a clinical trial. Collaborate with... ...agencies, or consultants, & coordinate the process to meet these requirements...OperationsFull timeWork at officeShift workWeekend work- Velocity Clinical Research, Inc. seeks a Clinical Research Coordinator I to manage trials per protocol and GCP. You will coordinate start-up, recruitment, data collection, and regulatory submissions while maintaining high standards of patient safety and data integrity....
- Velocity Clinical Research, Inc. is seeking a Clinical Research Coordinator I to conduct and manage clinical trials in accordance with study protocols, GCP, and Velocity SOPs. The role involves coordinating start-ups, recruitment, visits, data entry, and regulatory submissions...
- ...Children's Office of Academic Affairs and Career Development in Cincinnati, OH, is seeking a capable Clinical Research Coordinator to support complex, multi-center trials in the Allergy department. The role trains staff, ensures regulatory compliance, and coordinates...Full timeWork at office
- Cincinnati Children's in Cincinnati, OH, is seeking a Clinical Research Coordinator to manage study conduct across multiple active protocols in the... ..., assist with recruitment, and maintain essential trial documentation. The role requires coordinating with investigators...
- CTI Clinical Trial and Consulting Services is a global, privately held... ...-service clinical contract research organization (CRO) focused... ...Cincinnati, OH region with global operations in collaboration with... ...: The Clinical Project Coordinator position is responsible for...OperationsContract workWork experience placementWork at office
- CTI Clinical Trial and Consulting Services is seeking a Clinical Project Coordinator to support management efforts of Clinical Project Managers and Directors across all phases... ...’s in allied health and 1+ year of clinical research experience are required. #J-18808-Ljbffr CTIWork at office
- Cincinnati Children’s is seeking a collaborative professional to support Study Conduct/Clinical Research Practice. The role involves coordinating studies, preparing protocols and informed consents for IRB review, assembling supplies, collecting and labeling samples, and...Operations
- ...edge procedures and research that improves the health and clinical care of patients.... ...Research Professional II position to support... ...Center Clinical Trials Office (CTO). This... ...UC Health standard operating procedures. In conjunction... ...(if any). Order, coordinate, and schedule...Full timeWork experience placementWork at officeLocal areaFlexible hours
- Cincinnati Children's Hospital Medical Center is seeking a Clinical Research Coordinator to support study conduct in translational and clinical pharmacology. You will coordinate study materials, assist with IRB approvals, and manage data entry and regulatory documentation...OperationsFull time
- ...potential legal and business risks in operations, strategic planning, and business... ...appropriate outside counsel and oversee/coordinate outsourced legal work;Cross-... ...Medpace OverviewMedpace is a full-service clinical contract research organization (CRO). We provide Phase...OperationsContract workLocal areaWork from home
- ...best urban public research universities. Home... ...improves the health and clinical care of patients.... ...Professional II role. This position... ...Center Clinical Trials Office (CTO). Duties... ...Health standard operating procedures. Consent... ...clinical trials. Coordinate screening procedure...Hourly payWork experience placementWork at officeFlexible hours
- ...Children’s is seeking a day-shift, full-time professional in Psychiatry at the Burnet Campus to support clinical research operations. You will conduct studies, coordinate regulatory submissions, recruit participants, maintain communications with sponsors and teams, and...OperationsFull timeDay shift
$20 per hour
...Assistant to help support our clinical team and play an important... ...clinical testing Help coordinate daily clinical operations and support the medical... ...auto markets. Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple therapeutic areas...OperationsTemporary workLocal areaFlexible hoursWeekend work- ...companies and is continuing to add established Clinical Trial Managers and Project Managers with a... ...provide accountability for day-to-day operations of the project, as defined by the... ...direct supervision of project Clinical Research Associates and monitoring deliverablesQualificationsBachelor...OperationsContract workWork from home
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