Job Title

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 and support for Central Image Management Solution (CIMS) clinical trials. The role acts as a point of contact for issues and matters related to central reading with internal and external project teams, collaborates with stakeholders on document development, central reader training, and quality monitoring, and assists in analyzing image services and product offerings for CIMS clinical trials. The Associate supports the department and company in achieving objectives and strategic goals. Trials Management Support (30-40%) Act as point of contact for internal and external project teams for medical/scientific issues related to central reading. Interact with and/or elevate issues to Alimentiv''s 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, analyze and implement project-specific imaging requirements (e.g., quality control processes, central reading paradigms). 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 manuals). Assist in preparing and maintaining site training materials related to imaging standards and scoring indices based on scientific/medical information and/or practices. Central Reading Processes Support (30-40%) Assist with the development and/or review of central reader training materials specific to scoring and utilization of imaging systems. Participate in project- and non-project-specific central reader quality monitoring activities and training. Assist with regular and ad-hoc reviews of central reading statistical data outputs and/or raw data to identify issues and trends. Participate in developing mitigation strategies and process improvements related to central reading. Act as a point of contact for Alimentiv''s Medical Leadership regarding central reading issues and process improvements. Process and Product Design and Improvements (10-20%) Collaborate with cross-functional departments to evaluate, implement, and/or provide support for new imaging technologies and/or new or improved processes. Participate in developing and maintaining standard operating procedures, work instructions, and associated documents for central reading processes and standards. Participate in cross-functional imaging modality specific working groups and/or committees. Research and Development (10-20%) Collaborate with Alimentiv''s Medical Leadership and Scientific Advisors/Collaborators to assist in developing and maintaining Alimentiv''s standards for imaging and study design. Participate in developing and improving imaging processes related to trial imaging (e.g., central reading paradigms, quality control processes, central reader quality review monitoring). Contribute to the continuous improvement of Imaging Research and Development and the wider organization through information sharing, training, and education. Qualifications Minimum of a bachelor''s degree (specialization in Health/Life Sciences, Clinical Research or Medical Imaging preferred). Strong analytical and problemsolving skills. Excellent learning agility and ability to work in ambiguity. Accommodations for job applicants with disabilities are available upon request. #J-18808-Ljbffr