Imaging Research and Development Associate

The Imaging Research and Development Associate will assist with providing the Clinical Project Management, Data Management and Medical Leadership teams with medical, scientific, and operational advice/support for Central Image Management Solution (CIMS) clinical trials. Act as a point of contact assisting in issues/matters related to central reading with internal and external project teams. Collaborate with internal and external stakeholders on document development, central reader training and quality monitoring, and assist in analyzing image services and product offerings for CIMS clinical trials. Support the department and company in achieving objectives and strategic goals. \n Trials Management Support (30-40%) Act as point of contact for internal and external project teams for medical/scientific issues/matters related to central reading. Interact with and/or escalate issues to Alimentivs' Medical Leadership, Scientific Advisors/Collaborators, and/or Central Readers as needed. Participate in internal and Sponsor meetings as required. In collaboration with the project team, participate in analyzing and implementing project-specific imaging requirements (e.g., quality control processes, central reading paradigms, etc.). Lead the development of project-specific Image Review Charter(s) and if applicable, Central Reader Variability Monitoring documentation. Participate in the development of CIMS project-specific documents (e.g., Work Instructions, process flows, Instruction M

Responsibilities

• Act as point of contact for internal and external project teams for medical/scientific issues related to central reading
• Interact with and escalate issues to Alimentiv's Medical Leadership, Scientific Advisors/Collaborators, and Central Readers as needed
• Participate in internal and Sponsor meetings as required
• Analyze and implement project-specific imaging requirements including quality control processes and central reading paradigms
• Lead development of project-specific Image Review Charter(s) and Central Reader Variability Monitoring documentation
• Participate in development of CIMS project-specific documents such as Work Instructions and process flows
• Collaborate with internal and external stakeholders on document development, central reader training and quality monitoring
• Assist in analyzing image services and product offerings for CIMS clinical trials
• Support the department and company in achieving objectives and strategic goals