Clinical trial sponsors and sites are under pressure to separate hype from reality and identify where AI can deliver real value without compromising patient safety, data integrity or regulatory compliance. This webinar will examine how AI can be applied as a disciplined, pragmatic tool to support accelerating clinical trials in regulated environments.
The session begins with an AI framework grounded in clear guardrails for reliability, auditability and safety. The featured speakers will discuss how large language models can be paired with deterministic, expert-authored logic for data and actions, helping trial teams improve efficiency while maintaining appropriate oversight.
Attendees will also explore key expectations, concerns and non-negotiables for AI adoption, including transparency, human oversight and implementation guardrails. The session concludes with a look at how responsible innovation can shape future AI-enabled capabilities across clinical trial workflows.
Register for this webinar to learn how accelerating clinical trials depends on responsible AI, clear guardrails and regulated adoption.
Speakers
Priyanka Sharma, Senior Vice President, Software Engineering at Suvoda
Priyanka Sharma is Senior Vice President, Software Engineering at Suvoda and is responsible for all eClinical and eFinancial product development, testing and site reliability initiatives across the company. Prior to joining Suvoda, Priyanka oversaw conceptualization, architecture, resource management, requirements analysis, strategic planning, development and product launches for multiple business portfolios at IQVIA. She has extensive experience in regulated software solutions, clinical trial industry and compliance needs of the life sciences industry. In her past roles, she also established best practices, drove innovation and started high-performing teams across four continents for offerings deployed in 115+ countries. Priyanka holds a Master’s degree in Computer Science from India.
Jadon Sargent, Senior Product Owner For Suvoda IRT and Sofia
Jadon Sargeant serves as Senior Product Owner for Suvoda IRT and Sofia, the AI assistant on the Suvoda Platform. He champions innovation across mission-critical trial technologies, emphasizing reliability, teachability, scalability and data security. With a Master’s in Healthcare Systems Engineering, Jadon blends technical rigor with deep domain expertise and product leadership to deliver better trial experiences for sponsors, sites and patients. Prior to his current role, he collaborated closely with Suvoda customers on system implementation as a Services Project Manager.
Andrew McVeigh, Chief Architect, Suvoda
Andrew McVeigh is Suvoda’s Chief Architect responsible for product software architecture and design. He also leads the AI initiatives across the company, focusing on agentic and RAG support for integrating Suvoda’s clinical and financial data sources, and streamlining processes. Andrew has extensive experience in software architecture, having served as Chief Architect at Internet Scale companies such as LiveRamp and Hulu, and having led architecture designs for Amazon, Riot Games, UBS AG and the Amex Blue card platform. Andrew has a PhD in Software Engineering from Imperial College in London, where he wrote his thesis on software extensibility, and a Bachelor’s Degree with Honors in Electronics Engineering from the University of Western Australia.
Who Should Attend?
Ideal for Clinical Research professionals who are evaluating how to apply AI in a regulated trial environment without adding risk. Especially relevant for teams exploring AI-enabled platforms, eCOA and patient/site experience solutions that need clear guardrails for responsible innovation. Relevant areas of work include:
- Data Management
- Clinical Operations and Innovation
- Patient Engagement
- Site Enablement
- Digital Innovation
- Digital Transformation
- R&D IT
- Clinical Supply
- AI in Clinical Trials
What You Will Learn
Attendees will leave with a practical understanding of:
- How to evaluate AI solutions through the lens of reliability, safety and regulatory readiness
- Which AI use cases can genuinely reduce friction for sponsors and sites today, and where human expertise must remain in the loop
- How a platform-based, guardrail-driven approach can help trial teams adopt AI with confidence and sustain trust among patients, sites and sponsors
Xtalks Partner
Suvoda
Suvoda is a global clinical trial technology company with a market-leading, real-time software platform that empowers sponsors and CROs to make confident decisions and sites and patients to take calm, controlled action. Suvoda delivers interconnected, action-driven software solutions and industry-leading services and support, so that even in the most time-sensitive, mission-critical moments, life-changing studies keep moving forward. Headquartered outside Philadelphia, Suvoda also maintains offices in Portland, OR, Barcelona, Spain, Bucharest and Iasi, Romania, and Tokyo, Japan. The company maintains customer satisfaction scores that consistently exceed the technology industry average, contributing to the company being selected by trial sponsors and CROs to support more than 2000 trials across more than 95 countries. Suvoda recently merged with Greenphire, a leading provider of clinical trial financial management and patient support tools. To learn more, visit suvoda.com and follow Suvoda on LinkedIn.
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