Design, Data, and Decisions in Oncology Trials

• Gain lessons learned from common data and design pitfalls — and how to avoid them 
• Understand how thoughtful design and fit-for-purpose data strategies drive better decisions and reduce risk 

• Explore innovative design approaches, including external controls, adaptive methodologies, and biomarker-driven strategies 

• Discuss real-time data access and its impact on managing emerging data sources and complex protocols 

• Learn how data science techniques — including simulation — are shaping trial strategy and delivery 

• How to proactively spot and solve common challenges in oncology trial design and data execution 

• Ways to align design, data collection, and analytics from the outset 

• Emerging trial design innovations and when to use them 

• How to manage complex data streams in oncology 

• Chief Medical Officers 

• Clinical Operations and Clinical Development professionals 

• Program and Trial Leads 

• Data Managers 

• Biostatisticians 

• Clinical Scientists 

• Medical Directors 

• Regulatory Affairs professionals 

• Real-World Evidence (RWE) specialists 

• Data Scientists 

Who is this webinar for?
This webinar and panel discussion is designed for biotech and pharmaceutical leaders, clinical development professionals, biostatisticians, and clinical data scientists seeking actionable strategies to optimize oncology trials.

Will there be a recording available?
Yes, a recording will be provided to all registered attendees following the scheduled event.

Where can I get more information on the content presented?
To connect with the presenters, email info@mmsholdings.com and our team will connect you with the right person.