Required Attributes Bachelor's degree in a science or health related field
* Registered Technologist (R.T.) with advanced modality experience in CT, MRI or Nuclear Medicine required
* Proficiency in MS Office and internet applications required
* Minimum of 4 years of experience in medical imaging required...
* Minimum of 3 year of experience in the clinical trials industry preferred
* Knowledge of Good Clinical Practice (GCP), Quality Assurance/Compliance in a clinical trials setting is preferred
Knowledge of image trial documents is strongly preferred; i.e. Image Review Charter, Imaging Manual, Data Transmittal Forms, etc. RESPONSIBILITIES
* Perform technical quality review of images per trial specifications
* Perform Quantitative image analysis
* Perform imaging data reconciliation per trial specifications
* Manage research projects and early phase clinical trials for day-day activities
* Complete quality control documentation according to standard operating procedures
* Develop quality control documentation in conjunction with the Project Manager
* Generate, track, and resolve image queries to address technical issues in a timely manner
* Identify and assign cases reader for read assignment per the Standard Operating Procedure
(SOP)and the Study Specific Procedures (SSP)
* Prepare study dossiers to be associated with read assignment per the SOP/SSP
* Track the read assignment status and additional information in Clinical Trial Management Systems (CTMS)
experience
6show moreRequired Attributes Bachelor's degree in a science or health related field
* Registered Technologist (R.T.) with advanced modality experience in CT, MRI or Nuclear Medicine required
* Proficiency in MS Office and internet applications required
* Minimum of 4 years of experience in medical imaging required
* Minimum of 3 year of experience in the clinical trials industry preferred
* Knowledge of Good Clinical Practice (GCP), Quality Assurance/Compliance in a clinical trials setting is preferred
Knowledge of image trial documents is strongly preferred; i.e. Image Review Charter, Imaging Manual, Data Transmittal Forms, etc. RESPONSIBILITIES
* Perform technical quality review of images per trial specifications
* Perform Quantitative image analysis
* Perform imaging data reconciliation per trial specifications
* Manage research projects and early phase clinical trials for day-day activities
* Complete quality control documentation according to standard operating procedures
* Develop quality control documentation in conjunction with the Project Manager
* Generate, track, and resolve image queries to address technical issues in a timely manner
...
* Identify and assign cases reader for read assignment per the Standard Operating Procedure
(SOP)and the Study Specific Procedures (SSP)
* Prepare study dossiers to be associated with read assignment per the SOP/SSP
* Track the read assignment status and additional information in Clinical Trial Management Systems (CTMS)
experience
6show more
