Clinical Trial Imaging Specialist

Role & 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)
• Preferred candidate profile

Bachelors degree in a science or health related field

• Registered Technologist (R.T.) with advance modality experience in CT, MRI or Nuclear Medicine required
• Proficiency in MS Office and internet applications required
• Minimum of 2 years of experience in medical imaging required
• Minimum of 1 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 strongly preferred; i.e. Image Review Charter, Imaging Manual, Data Transmittal Forms, etc

Email : [email removed]