Empowering Clinical Research Through RBQM Innovation

Mark your calendars for November 7th as we bring you #RO24, a virtual event featuring some of the industry's most experienced RBQM influencers. Designed to help clinical research Sponsors and CROs navigate the ever-evolving world of Risk-Based Quality Management (RBQM), this event offers something for everyone—whether you're new to RBQM or looking to deepen your expertise—with two focused tracks led by top experts in the field.

Why Attend

  • Comprehensive RBQM Strategies: Explore two focused tracks designed to address both foundational knowledge and advanced RBQM practices.
  • Real-World Case Studies: Discover practical applications of RBQM through detailed customer case studies that offer actionable takeaways.
  • Stay Ahead of the Curve: Understand the latest trends and innovations driving the future of clinical research and how RBQM is shaping that future.
  • Networking Opportunities: Connect with peers, industry experts, and like- minded professionals to exchange ideas and experiences in RBQM
  • Tailored Content for All Levels: Whether you're just starting with RBQM or seeking to refine your expertise, the event provides valuable content for all experience levels.

Agenda

Paskaitų programa

November 7, 2024 14:00

Introduction and Welcome

Duncan Hall
Chief Executive officer, TRI

November 7, 2024 14:15

Keynote: Trends in Global Clinical Trials and how the UK is adapting to meet the needs of Sponsors and patients

Michael Lewis
Scientific Director for Innovation, NIHR

November 7, 2024 14:45

Why RBQM is urgent as well as important

Duncan Hall
Chief Executive officer, TRI

November 7, 2024 15:15

What’s driving clinical data innovation

Richard Young
Vice President, Clinical Data Strategy, Veeva Systems

November 7, 2024 15:45

Moving from Sponsor to CRO

Shawntel Swannack
Head, Risk Based Quality Management, Emmes

November 7, 2024 16:15

How RBQM generates new business for CROs

Eithne Connolly
Associate Director, Worldwide Clinical Trials

November 7, 2024 16:45

Operationalizing RBQM Customer Case Study

Karen McCarthy Schau
Senior Director, Clinical Data Management at Vertex Pharmaceuticals

November 7, 2024 17:15

Panel Discussion: The future of RBQM

Richard Young
Vice President, Clinical Data Strategy, Veeva Systems

Eithne Connolly
Associate Director, Worldwide Clinical Trials

Duncan Hall
Chief Executive officer, TRI

Michael Lewis
Scientific Director for Innovation, NIHR

Karen McCarthy Schau
Senior Director, Clinical Data Management at Vertex Pharmaceuticals

November 7, 2024 14:00

Introduction and Welcome

Duncan Hall
Chief Executive officer, TRI

November 7, 2024 14:15

Keynote: Trends in Global Clinical Trials and how the UK is adapting to meet the needs of Sponsors and patients

Michael Lewis
Scientific Director for Innovation, NIHR

November 7, 2024 14:45

Where do I start?

Imogen Bates
RBQM Operations Consultant II, TRI

November 7, 2024 15:15

How do I conduct my first protocol risk assessment?

Rob Gray
RBQM Operations Consultant, TRI

November 7, 2024 15:45

How does my risk assessment influence my KRI and QTL selection?

Laura Illingworth
Statistician, TRI

Isabel Villanueva
RBQM Operations Consultant, TRI

November 7, 2024 16:15

Managing Risks Customer Case Study

TBC

November 7, 2024 16:45

Central Monitoring Customer Case Study

TBC

November 7, 2024 17:15

Panel Discussion: The future of RBQM

Duncan Hall
Chief Executive officer, TRI

Richard Young
Vice President, Clinical Data Strategy, Veeva Systems

Michael Lewis
Scientific Director for Innovation, NIHR

Karen McCarthy Schau
Senior Director, Clinical Data Management at Vertex Pharmaceuticals

Eithne Connolly
Associate Director, Worldwide Clinical Trials

Speakers

Duncan Hall

Chief Executive officer, TRI
Read Bio

Michael Lewis

Scientific Director for Innovation, NIHR
Read Bio

Richard Young

Vice President, Clinical Data Strategy, Veeva Systems
Read Bio

Shawntel Swannack

Head, Risk Based Quality Management, Emmes
Read Bio

Eithne Connolly

Associate Director, Worldwide Clinical Trials
Read Bio

Karen McCarthy Schau

Senior Director, Clinical Data Management at Vertex Pharmaceuticals
Read Bio

Imogen Bates

RBQM Operations Consultant II, TRI
Read Bio

Rob Gray

RBQM Operations Consultant, TRI
Read Bio

Laura Illingworth

Statistician, TRI
Read Bio

Isabel Villanueva

RBQM Operations Consultant, TRI
Read Bio

Neshad Sharma

Lead of RBQM Leaders - Bayer
Read Bio

Laura Tebbs

Clinical Operations Manager - Roche
Read Bio

Frequently Asked Questions


Yes, you will need to enter your name and email address to enjoy all RBQM Operations 2024 Virtual Event features.
Your login details will be emailed to you ahead of the event. You can use these details to access the online event.
The event will remain open 24/7 for 30 days. Therefore, you can attend whenever it’s convenient for you during this period of time.
This is an online event. You do not have to travel to any specific location. You can participate anywhere that you have Internet access. The event is accessible from desktop, mobile and tablet devices.
Yes. Like any physical event, we will have a Swag bag for you! You can add all of the documents available to the online Swag bag in your account and then email them to yourself or share items with colleagues and friends by simply entering their email.
Absolutely. We are counting on you to invite others! Help us spread the word. You can simply share the link to this page, and they can register at their convenience.
NO. You do not need to download or install any software to participate in our conference. You only need to have access to the Internet.