AI Futurescape: Unpacking Perceptions and Implications in Clinical Trials

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Registration for the webinar

Currently there are no future dates for the webinar.

Moderators

Moderator 1 of the webinar: Keith Dorricott

Keith Dorricott

Keith has been a qualified Lean Six Sigma Master Black Belt since 2007. He has a solid background in the practical use of process improvement, business process re-engineering, and metrics in clinical trials. Having a wealth of experience across processes in clinical trials and being a frequent speaker at conferences such as SCOPE and the MCC Summit, Keith helps make the complex understandable. In his spare time, he also facilitates and provides thought leadership for workgroups at the MCC, such as Centralized Monitoring, eCOA, and Vendor Oversight.

Moderator 2 of the webinar: Nechama Katan

Nechama Katan

Nechama stands at the forefront of AI-driven data analytics, serving as the Chief Wicked Problem Wizard at Wicked Problem Wizards. Concurrently, at Pfizer, Nechama has assumed pivotal roles such as Director of Innovative Data Analytics and Associate Director Central Monitoring Lead. In this capacity, she has been instrumental in spearheading projects that seamlessly integrate AI and ML solutions, notably in Pfizer's Risk-Based Data Management initiatives.

Moderator 3 of the webinar: Adam Baumgart

Adam Baumgart

Adam is a clinical development leader with over 34 years of experience in the pharma industry and 23 years leading departments and projects. He has led two major RBQM company transformations and the resulting organizational implementation of structures, roles, processes and supporting software. Adam has broad experience in clinical data management, programming, site monitoring, and study leadership and is a certified Lean Six Sigma Green Belt and Certified Project Manager.

Moderator 4 of the webinar: Linda Bunschoten

Linda Bunschoten

Linda, CMO at Cyntegrity, brings a broad range of international industry experience. In her 25+ year career in the healthcare industry, she has supported clients, KOLs, direct operations and distributors representing over 100 countries to achieve their growth goals. Linda's expertise include translating insights into strategy and ensure that cross- departmental activities contribute to the overall business goals and meet the industry's high-quality expectations.

June 26, 2024 Michal Helbin

A comprehensive approach to the management of risks in a clinical study. The platform is very well designed, it has been very well presented during the webinar. The platform is detailed but graphically appealing. It utilizes the smart risk categories as proposed by the TransCelerate Biopharma, uses some proprietary tools and knowledge as designed by the Cyntegrity and is easily scalable should any organization need to add more categories at any time. Its a product well done.

October 22, 2025 Naomi Bossman

I appreciate the expertise and interpersonal dynamic of the presenters/moderator, as well as, examples, lessons learned, exercises, and ability to learn from other's experiences. Big fan of Cyntegrity! Thank you for hosting these webinars.

November 12, 2025 Mary Banach

Thank you - This webinar was exactly what is needed in the CDM Community. Mary Banach Chair DIA CDM Community

AI Futurescape: Unpacking Perceptions and Implications in Clinical Trials

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ABOUT THIS VIRTUAL EVENT

Artificial Intelligence (AI) is transforming the landscape of clinical trials, offering unprecedented possibilities yet raising critical ethical questions. This dynamic, two-day event—comprising multiple sessions totaling 5 hours—provides a comprehensive platform for such discussions. As pioneers in intelligent data science solutions, we invite you to join us for a deep dive into AI's revolutionary and contentious role in clinical trials.

Our event aims to serve as a meeting ground for professionals across the spectrum—those excited by AI's transformative potential and those concerned about its ethical ramifications. We'll cover topics from how AI is optimizing trial protocols to the very real concerns about job security in an AI-driven landscape.

By pre-registering, you're taking a crucial step towards being a founding member of a groundbreaking Life Science community focused on Responsible AI. Your insights will not only shape a vital industry-wide dialogue but also help define the path toward Responsible AI, benefiting all stakeholders — from patients to providers, regulators to vendors. Together, let's address the challenges and seize the opportunities that AI presents, crafting guidelines and best practices that will steer the future of clinical trials in a direction that's both innovative and ethical.


WHY PRE-REGISTER?

- Express your interest and be first in line for an official invitation (non-binding)

- Receive a detailed event and speaker outline in the first week of November

- Contribute to a crucial dialogue on Responsible AI

Note: Pre-registration does not guarantee a seat and is non-binding. The event details will be outlined in the official invitation.


WHO SHOULD ATTEND?

This event is ideal for clinical researchers, data scientists, BioPharma and clinical R&D IT professionals, patient and vendor representatives, policymakers, and anyone interested in the evolving role of AI in clinical trials.

Secure your spot today and be a part of this engaging virtual event.


SHARE YOUR INSIGHTS

We invite you to share your invaluable insights through our 10-minute survey. The aggregated results will be presented at the event, giving you a unique opportunity to influence the dialogue and shape the future of AI in this critical field: https://www.surveymonkey.com/r/AI-in-Clinical-Trials

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