Trauma PI Coordinator

Description:RESPONSIBLE FOR:The Trauma Performance Improvement (PI)Coordinator, in collaboration with Trauma Acute Care Surgery (TACS)Leadership, is responsible for the Trauma Performance Improvementand Patient Safety (PIPS) program. The Trauma PI Coordinator worksclosely with the Trauma Medical Director, Trauma Program Managerand the Trauma Registrar(s) to...

Description:RESPONSIBLE FOR: The Trauma Performance Improvement (PI) Coordinator, in collaboration with Trauma Acute Care Surgery (TACS) Leadership, is responsible for the Trauma Performance Improvement and Patient Safety (PIPS) program. The Trauma PI Coordinator works closely with the Trauma Medical Director, Trauma Program Manager and the Trauma...

Description:RESPONSIBLE FOR: The Trauma Performance Improvement (PI) Coordinator, in collaboration with Trauma Acute Care Surgery (TACS) Leadership, is responsible for the Trauma Performance Improvement and Patient Safety (PIPS) program. The Trauma PI Coordinator works closely with the Trauma Medical Director, Trauma Program Manager and the Trauma...

Description:RESPONSIBLE FOR: The Trauma Performance Improvement (PI) Coordinator, in collaboration with Trauma Acute Care Surgery (TACS) Leadership, is responsible for the Trauma Performance Improvement and Patient Safety (PIPS) program. The Trauma PI Coordinator works closely with the Trauma Medical Director, Trauma Program Manager and the Trauma...

Description: RESPONSIBLE FOR: The Trauma Performance Improvement (PI) Coordinator, in collaboration with Trauma Acute Care Surgery (TACS) Leadership, is responsible for the Trauma Performance Improvement and Patient Safety (PIPS) program. The Trauma PI Coordinator works closely with the Trauma Medical Director, Trauma Program Manager and the Trauma...

Description:RESPONSIBLE FOR: The Trauma Performance Improvement (PI) Coordinator, in collaboration with Trauma Acute Care Surgery (TACS) Leadership, is responsible for the Trauma Performance Improvement and Patient Safety (PIPS) program. The Trauma PI Coordinator works closely with the Trauma Medical Director, Trauma Program Manager and the Trauma...

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Screen reader users may encounter difficulty with this site. For assistance with applying, please contact hr-accessibleapplication@osu.edu. If you have questions while submitting an application, please review these frequently asked questions. Current Employees and Students: If you are currently employed or enrolled as a student at The Ohio State...

Overview The Clinical Research Coordinator's primary responsibility is managing elements of clinical studies in order to meet all protocol obligations while following International Council on Harmonization of Technical Requirements/Good Clinical Practice(ICH/GCP) guidelines; and departmental/institutional standard operating procedures. These elements...

Job DescriptionJob DescriptionPOSITION SUMMARY: This position is primarily responsible to contact persons referred for services within 24 hours. Implements strictly FSOH no wait time policy. Conducts initial intake activities according to FSOH protocol.Conducts a thorough assessment and completes a Diagnostic Assessment report. The assessment must reflect...

Overview The Center for Injury Research and Policy contributes to the National Electronic Injury Surveillance System (NEISS) of the U.S. Consumer Product Safety Commission (CPSC) as one of only eight pediatric hospital reporting sites among a network of 100 hospitals nationally. More than 20,000 children are treated for an injury in the emergency department...

Overview The Clinical Research Coordinator II's primary responsibility is managing all of the elements of a clinical study in order to meet all protocol obligations while following ICH/GCP guidelines; and departmental/institutional standard operating procedures. These elements include but are not limited to; start-up activities, launch activities, day to...

Overview The Clinical Research Coordinator I is responsible for managing elements of a clinical study in order to meet all protocol obligations while following ICH/GCP guidelines; and departmental/institutional standard operating procedures. These elements include but are not limited to; start-up activities, launch activities, day to day management of a...

Screen reader users may encounter difficulty with this site. For assistance with applying, please contact hr-accessibleapplication@osu.edu. If you have questions while submitting an application, please review these frequently asked questions.Current Employees and Students:If you are currently employed or enrolled as a student at The Ohio State University,...

Overview The Research Faculty Transition and Integration Coordinator is responsible for executing research-based faculty onboarding, integration, and off-boarding activities. Provides an assortment of concierge services to new faculty members including move coordination, equipment management, lab planning, recruiting staff, assisting with IRB/IACUC/IBC...

About the Role The Clinical Research Coordinator (CRC) is responsible for conducting and documenting clinical research and trials for the Research Division while adhering to Good Clinical Practice/ICH Guidelines and the Code of Federal Regulations. What You'll Be Doing Administratively and clinically coordinates a team to effectively conduct a minimum six...

Screen reader users may encounter difficulty with this site. For assistance with applying, please contact hr-accessibleapplication@osu.edu. If you have questions while submitting an application, please review these frequently asked questions.Current Employees and Students:If you are currently employed or enrolled as a student at The Ohio State University,...

Overview The Clinical Research Coordinator II is responsible for managing all of the elements of a clinical study in order to meet all protocol obligations while following ICH/GCP guidelines; and departmental/institutional standard operating procedures. These elements include but are not limited to; start-up activities,launch activities, day to day...

Overview The Clinical Research Coordinator I is responsible for managing elements of a clinical study in order to meet all protocol obligations while following ICH/GCP guidelines; and departmental/institutional standard operating procedures. These elements include but are not limited to; start-up activities, launch activities, day to day management of a...

Overview The Nahata Lab is looking for a Clinical Research Coordinator II to support our mission of providing efficient coordination of diverse behaviorally-focused clinical research, including behavioral intervention trials and observational research. The Clinical Research Coordinator II is responsible for managing all of the elements of a clinical study...