Imaging Research And Development Associate

Summary

Join Alimentiv as an Imaging Research and Development Associate and provide medical, scientific, and operational support for Central Image Management Solution (CIMS) clinical trials. You will act as a point of contact for central reading issues, collaborate with internal and external stakeholders on document development and training, and analyze image services. Responsibilities include trials management support, central reading processes support, process/product design and improvements, and research and development. The role requires a Bachelor's degree (preferably in Health/Life Sciences, Clinical Research, or Medical Imaging), strong analytical and problem-solving skills, and excellent learning agility. The position is remote-based and offers a competitive salary plus bonus.

Requirements

• 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

Responsibilities

• Act as a 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 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, 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
• 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 Alimentiv’s Medical Leadership regarding central reading issues, process improvements, etc
• 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
• Collaborate with Alimentiv’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

Preferred Qualifications

Specialization in Health/Life Sciences, Clinical Research or Medical Imaging

Benefits

• Remote-based
• $59,500 - $99,500 a year
• + Bonus
• Accommodations for job applicants with disabilities are available upon request