Imaging is one of the most complex yet underestimated components of modern clinical trials. While imaging endpoints provide critical insights for regulatory approval and patient outcomes, many Clinical Operations leaders experience blind spots in planning, execution and vendor management. Without the right strategy, these gaps can cause delays, budget overruns and compromised data quality.
This webinar will provide a practical framework for navigating the nuances of implementing an imaging strategy in clinical trials. Drawing from real-world experience, the discussion will highlight common pitfalls, from protocol design through site management and data submission, and explore strategies to anticipate challenges before they arise.
The featured speakers will also discuss the evolving role of emerging technologies, such as artificial intelligence (AI) and large language models (LLMs), in imaging workflows, as they help teams streamline data handling and enhance trial efficiency.
The session will also include a unique real-world use case, offering an inside look at how imaging challenges were successfully addressed in practice and what lessons Clinical Operations leaders can take forward. By the end of the webinar, participants will be better equipped to identify blind spots in their imaging strategies, apply practical solutions and strengthen collaboration with imaging service providers.
Register for this webinar to gain actionable insights into building and strategizing imaging in clinical trials to minimize risk, reduce delays and set the stage for smarter trials.
Speakers
Diandra Donald, Project Manager II, Median Technologies
With over five years of experience in clinical research within the field of medical imaging, Diandra Donald has a proven track record of successfully leading late-phase and retrospective oncology trials across Europe and North America. She brings strong expertise in advanced imaging modalities, including CT, MRI, echocardiograms and FDG PET, and is well-versed in imaging criteria such as RECIST 1.1, iRECIST, LUGANO and volumetric assessments.
Diandra holds a PMP® certification in project management, underscoring her ability to drive complex clinical studies with precision and strategic oversight. She ensures studies run efficiently from start-up through close-out, combining seamless client communication with a commitment to operational excellence.
Jessica Bell, Senior Solutions Consultant, AG Mednet
Jessica Bell is a Senior Solutions Consultant at AG Mednet, bringing in more than 15 years of experience in clinical research with a focus on medical imaging and project management. She spent over a decade at CROs, where she managed the imaging components of global clinical trials and gained deep expertise in operational delivery across oncology and other therapeutic areas.
Before joining AG Mednet, Jessica spent five years managing Trial Delivery, overseeing diverse portfolios and ensuring studies met operational, quality and regulatory standards. At AG Mednet, she leverages her combined background in imaging and technology to help sponsors and CROs implement software solutions that streamline trial workflows, reduce risk and improve data quality.
Her unique perspective, spanning both the service and technology sides of imaging, makes her a trusted partner for clinical teams navigating complex studies.
Message Presenter
Catherine Tyner, Head of Clinical Strategy, AG Mednet
Catherine Tyner brings 27 years of clinical research experience with a focus on Oversight Group Management for Clinical Endpoint Committees, Data Monitoring Committees and other operations. Throughout her career, Ms. Tyner has led and developed oversight departments at Quintiles (now IQVIA), Novella Clinica and Covance (now Fortrea), providing strategic management for over 500 clinical trials, including complex megatrials across diverse therapeutic areas. A recognized thought leader in endpoint adjudication best practices, Ms. Tyner has authored the industry’s seminal guidance on adjudication operations and best practice. In her new role at AG Mednet, Ms. Tyner will work to expand and tailor the value jointly created with new and existing CROs, Trial Sponsors, Core Labs and Academic Research Organizations, working closely to optimize the future of clinical process efficiency.
Message PresenterWho Should Attend?
This webinar will appeal to:
- Clinical Operations leaders
- Clinical Trial Managers and Directors
- Project Managers working on trials with imaging endpoints
- Medical Directors and Clinical Development leaders
- ARO and CRO professionals supporting imaging-based studies
What You Will Learn
Attendees will gain insights into:
- How to recognize and address common blind spots in clinical trial imaging strategy
- Practical approaches for managing imaging workflows, including site qualification, training and data submission
- Best practices for partnering effectively with imaging service providers as an extension
- Where emerging technologies such as AI and LLMs can support and streamline imaging operations
- Lessons learned from a real-world use case demonstrating imaging strategy in action
Xtalks Partner
AG Mednet
AG Mednet is a leading provider of intelligent technology solutions for clinical trial operations, medical affairs, and safety. Judi, the company’s flagship cloud-based platform, and tailored services, are designed to reduce operational complexity, ensure regulatory compliance, and improve data integrity across global studies, empowering sponsors, CROs, and sites to streamline journeys and accelerate timelines.
With expertise across more than 20 therapeutic areas, including oncology, cardiology, neurology, and rare diseases, AG Mednet has over two decades of experience optimizing clinical trial processes, with trusted, proven use cases for integrated DSMB/oversight management, eligibility assessment, remote monitoring, site and user qualification, 24×7 medical monitoring, and is the industry standard for endpoint adjudication, compliant DICOM imaging collection, storage, and review.
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