As clinical trial data grows in volume and complexity, traditional approaches to data review and cleaning are becoming increasingly difficult to sustain. Risk-based data management (RBDM) offers a more focused approach, helping teams prioritize critical data, identify risks earlier, and improve oversight throughout the clinical trial lifecycle.  

Join MMS experts Doreen Van Huyssteen, Director, Clinical Data Management and Lucy Sutton, Vice President, Account Management, for a discussion exploring the practical realities of implementing RBDM, the success factors that drive meaningful outcomes, and how evolving technologies may shape the future of data oversight.  

Whether you’re currently implementing risk-based approaches or evaluating how to modernize your data management strategy, this webinar will provide practical insights and forward-looking perspectives from industry experts.  

Speakers 

Doreen Van Huyssteen, Director, Clinical Data Management 
Lucy Sutton, Vice President, Account Management  

Watch This Webinar To:  

During this webinar, we will discuss: 

  • Learn why risk-based data management is gaining momentum across the industry  
  • Explore the key success factors for effective RBDM, including governance, cross-functional collaboration, process adaptation, critical-to-quality data tiering, and technology enablement 
  • Understand how successful organizations establish ownership, governance structures, and dynamic risk review processes 
  • Identify practical approaches for applying data tiering and focusing effort where it matters most 
  • Discover what sponsors should look for when evaluating RBDM technologies and data visualization tools 
  • Gain practical recommendations for organizations looking to strengthen or refine their current RBDM strategy 

What You Will Learn:

Risk-based approaches are no longer optional. Growing data volumes, increasingly complex study designs, regulatory expectations, and pressure to improve efficiency are driving organizations to rethink how they manage clinical trial data. 

This webinar will provide actionable insights into: 

  • Focusing resources on critical data and risk areas 
  • Improving cross-functional collaboration and oversight 
  • Building repeatable, scalable governance processes 
  • Leveraging technology effectively without becoming tool-dependent 
  • Preparing for the next generation of risk-based oversight 

Topics We’ll Explore:

  • Why risk-based data management is becoming increasingly important as clinical trial data volumes, complexity, and regulatory expectations continue to grow 
  • The foundational success factors behind effective RBDM, including governance, ownership, cross-functional collaboration, process adaptation, and data tiering 
  • What successful implementation looks like in practice, from dynamic risk assessments and review meetings to proactive oversight and decision-making 
  • How sponsors can apply critical-to-quality principles to focus resources on the data and risks that matter most 
  • What to look for when evaluating data management and visualization tools, and why process and governance should come before technology selection 
  • How technologies such as dashboards, advanced analytics, machine learning, and AI are supporting more proactive risk detection and oversight 
  • The evolving role of RBDM within broader risk-based quality management frameworks 
  • Where human expertise remains essential, even as automation and AI capabilities become more advanced 

Who Will Benefit From Attending?

This webinar is designed for professionals involved in clinical trial oversight, including: 

  • Clinical Data Management 
  • Biometrics and Biostatistics 
  • Clinical Operations 
  • Data Science 
  • Quality and Risk Management 
  • Regulatory and Study Oversight Stakeholders 
  • Sponsor teams seeking to improve data quality, oversight, and operational efficiency through risk-based approaches 

FAQs

Is this webinar available on demand?
Yes. Register to access the webinar anytime.

Who should watch this webinar?
This session is ideal for clinical data management, biometrics, clinical operations, quality, regulatory, and sponsor teams involved in clinical trial oversight.

What practical insights will I gain?
Learn proven strategies for implementing risk-based data management, improving governance, prioritizing critical data, and leveraging technology for smarter oversight.

Is there a cost to attend?
No. This webinar is complimentary, and registration is free for all attendees.

Meet our Speakers
Doreen Van Huyssteen
Director, Clinical Data Management Biometrics
Lucy Sutton
Vice President, Account Management

Register Now