Clinical Trial Imaging Specialist

Job description

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 : monisha.lahiri@randstad.in