Imaging Research and Development Associate

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 Manuals, etc.).
  • Assist in the preparation and maintenance of 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 trainings.
  • Assist with regular and ad-hoc reviews of central reading statistical data outputs and/or raw data to identify issues/trends.
  • Participate in the development of mitigation strategies and process improvements related to central reading.
  • Act as a point of contact for Alimentivs’ Medical Leadership regarding central reading issues, process improvements, etc.

Process/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/improved processes.
  • Participate in the development and maintenance of 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 Alimenitv's Medical Leadership and Scientific Advisors/Collaborators to assist in the development and maintenance of Alimentiv's standards for imaging and study design.
  • Participate in the development and/or improvements of imaging processes related to trial imaging (e.g., central reading paradigms, quality control processes, central reader quality review monitoring, etc.).
  • 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 problem-solving skills
  • Excellent learning agility and ability to work in ambiguity

Working Conditions

• • Remote-based