Imaging Specialist

Summit Therapeutics • Princeton, NJ

5d • $77,000 - $91,000

About The Position

The Imaging Specialist will be responsible for tracking images and interacting with Summit, CRO and site stakeholders to maintain workflow of imaging procedures and quality of study deliverables across multiple clinical trials. This position will be responsible for supporting compliance with imaging protocols, managing workflows, and driving quality standards for imaging deliverables.

Requirements

• Bachelor’s degree in a related field (e.g., Life Sciences, Radiology, Biomedical Engineering, Clinical Research) or equivalent experience.
• A minimum of 3+ years of experience in clinical imaging coordination, radiology, or clinical trial operations within the pharmaceutical, biotech, or CRO industry.
• Demonstrated ability to apply specialized knowledge in imaging science to clinical trial operations.
• Experience in managing imaging vendors, imaging core labs, and Independent Review Committees (IRC).
• Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) systems, and imaging analysis software is preferred.
• Ability to work independently and exercise sound judgement in a fast-paced, deadline-driven environment while maintaining high attention to detail.
• Excellent communication, problem-solving, and organizational skills to collaborate effectively with cross-functional teams.

Responsibilities

• Assist the Senior Imaging Coordinator to track imaging metrics to ensure timely delivery of all imaging related deliverables.
• Lead the coordination and oversight of imaging workflows across clinical trials, ensuring alignment with protocol requirements and regulatory standards.
• Manage and track image collection and query response with Vendors to ensure timely retrieval of study related data.
• Assist Senior Imaging Coordinator to manage all scan collections for Independent Review Committee Assessments.
• Develop and maintain imaging metrics dashboards and reports to monitor performance and ensure timely delivery of imaging data.
• Review imaging documents such as imaging specifications and project plans as they relate to assigned clinical trials
• Able to function well in a high-paced environment.
• Effectively communicate across functions of the study team and solve imaging issues as it relates to study activities
• All other duties as assigned

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level