Call for Abstracts
We’re now accepting abstract submissions for 2025 Research Revolution. This is your chance to share your ideas, lessons learned, and real-world innovations with an audience of industry peers shaping the future of clinical research.
What we’re looking for:
Session abstracts focused on practical strategies, bold ideas, and results-driven innovations in trial operations, collaboration, and technology.
What you’ll get:
- A complimentary pass to the Research Revolution
- A platform to showcase your leadership and expertise
- The chance to inspire change across the research community
Submit your abstract by May 15.
Our expert panel will review submissions and notify selected speakers shortly after.
Our expert panel will review submissions and notify selected speakers shortly after.
Take a look at last year's agenda
While we’re finalizing the 2025 agenda, let’s take a look back at the Research Revolution 2024 agenda. We forged the pathway to connection through our tracks: collaboration, change management, connectivity and customer knowledge.
2024 Agenda
Monday, October 7th
8:00am - 9:00am
Breakfast + Networking
Enjoy a full breakfast and networking before the day begins.
9:00am - 9:50am | Keynote
Shaping the Future of Clinical Trials: A Roadmap for Innovation and Efficiency
This keynote will explore the transformative journey towards improving trial operations and site enablement, reflecting on broader industry challenges and technological solutions. We will discuss the importance of strategic investments in technology and the role collaborative platforms play in overcoming operational hurdles. In this session, you will gain insight into the principles of designing user-centric technology that streamlines processes, ensures data integrity, and promotes efficiency across clinical trial ecosystems.
10:00am - 10:50am | Keynote
Beyond Boundaries: The Globalization of Clinical Trials
Globalization presents both opportunities and complexities for clinical trial operations. This keynote will delve into the trends, challenges, and strategies for conducting multi-national clinical trials. Topics will include navigating regulatory landscapes, ethical considerations in diverse populations, leveraging global data for better outcomes, and the role of technology in bridging geographical gaps. Attendees will gain valuable insights into how to effectively manage and capitalize on the globalization of clinical trials to accelerate drug development and reach more diverse patient populations.
11:00am - 11:50am | Keynote
The Next Frontier: Integrating Emerging Technologies into Clinical Trials
In this forward-looking keynote we will explore the future of clinical trials through the lens of emerging technologies such as artificial intelligence, blockchain, wearable devices, and more. The session will offer a glimpse into how these technologies are set to revolutionize trial design, patient engagement, data security, and real-time monitoring. With a focus on practical applications and the roadmap for integration, it will inspire attendees to embrace innovation, highlighting the benefits and considerations for a technology-driven approach to clinical trials.
12:00pm - 1:30pm
Lunch + Networking
Enjoy a full lunch and networking opportunities.
1:30pm - 2:15pm | Breakouts
Navigating the Future of Clinical Trials: A Regulatory Update for 2024 and Beyond
This session provides a comprehensive overview of the latest regulatory changes and guidelines affecting clinical trials globally. Experts will discuss the implications of these updates for trial design, execution, and compliance, and offer strategies for staying ahead in a rapidly evolving regulatory landscape.
Harnessing AI and Machine Learning for Enhanced Trial Efficiency
Explore how artificial intelligence (AI) and machine learning (ML) are revolutionizing clinical trial operations. This session will cover practical applications of AI and ML in trial design, patient recruitment, data analysis, and risk management. Learn from case studies demonstrating the tangible benefits of these technologies in reducing trial times and improving outcomes.
Improving Site Selection and Management: Strategies for Success
Selecting and managing clinical trial sites are critical components of trial success. This session will cover strategies for effective site selection, the importance of site and investigator relationships, and how to manage sites for optimal performance, including technology tools that can aid in site management and communication.
Florence Users Session
TBD: A session designed for users of the Florence Site Enablement Platform
2:30pm - 3:15pm | Breakouts
Adaptive Trial Designs: Flexibility and Efficiency in Clinical Research
Adaptive trial designs offer a flexible approach to clinical research, allowing modifications to the trial after it has started without compromising its integrity. This session will discuss the types of adaptive designs, their benefits, regulatory considerations, and how they can make clinical trials more efficient and effective.
Ethical Considerations in Clinical Trial Operations: Protecting Participants in a Digital Age
As technology advances, so do the ethical considerations surrounding clinical trial operations. This session addresses the complexities of participant privacy, data security, and informed consent in the digital age. Join a panel of ethicists, legal experts, and industry leaders for a critical discussion on maintaining the highest ethical standards in your trials.
Clinical Trial Workforce Development: Navigating the Digital Transformation
As clinical trials increasingly embrace digital technologies, the need for a skilled workforce has never been more critical. This session will explore strategies for developing a tech-savvy clinical trial workforce, including training programs, leadership development, and fostering a culture of continuous learning. Attendees will learn how to equip their teams with the necessary tools and knowledge to excel in the digital age of clinical research.
Florence Users Session
TBD: A session designed for users of the Florence Site Enablement Platform
3:30pm - 4:15pm | Breakouts
Global Clinical Trials: Navigating International Regulations and Logistics
Conducting clinical trials on a global scale presents unique challenges, including navigating diverse regulatory landscapes and managing complex logistics. This session will provide insights into successful international trial management, including regulatory harmonization, cultural considerations, and logistical strategies to ensure trial success across borders.
Sustainability in Clinical Trials: Towards Greener Operations
As the focus on environmental sustainability intensifies, this session explores how clinical trials can minimize their environmental footprint. Discussions will cover sustainable trial design, waste reduction strategies, and the adoption of green technologies. Learn how making your trials more sustainable can also drive efficiency and cost savings.
Remote Monitoring Strategies: Ensuring Quality and Compliance from Afar
This session will dive into the best practices and innovative approaches for remote monitoring of clinical trial sites. Experts will share insights on leveraging technology to maintain rigorous data quality, ensure regulatory compliance, and foster effective communication between sponsors, CROs, and sites. The discussion will include tips on selecting the right tools, addressing common challenges, and examples of successful remote monitoring implementations.
Florence Users Session
TBD: A session designed for users of the Florence Site Enablement Platform
4:30pm - 5:00pm
Game Show
Join us for our annual game show! You won’t wan to miss this half hour of fun and entertainment to end the day.
7:30pm - 10:30pm
After Party
After grabbing dinner, join us for our after party!
Tuesday, October 8th
8:00am - 9:00am
Breakfast + Networking
Enjoy a full breakfast and networking before the day begins.
9:00am - 9:50am | Keynote
Navigating Digital Transformation in Clinical Trials: A Roadmap for Change Management
Digital transformation is essential for modernizing clinical trials but requires effective change management to succeed. This session offers a comprehensive roadmap for managing the transition to digital operations, focusing on stakeholder engagement, training, and overcoming resistance to ensure a smooth and successful implementation.
9:00am - 10:50am | Breakouts
Cybersecurity in Clinical Trials: Safeguarding Data in a Digital World
Conducting clinical trials on a global scale presents unique challenges, including navigating diverse regulatory landscapes and managing complex logistics. This session will provide insights into successful international trial management, including regulatory harmonization, cultural considerations, and logistical strategies to ensure trial success across borders.
Florence Executive Advisory Board
Members of the Florence Executive Advisory Board will convene for a strategic session.
11:00am - 11:50am | Breakouts
Ensuring Data Integrity: The Keystone of AI and ML in Clinical Trials
In the age of Artificial Intelligence (AI) and Machine Learning (ML), the adage “garbage in, garbage out” has never been more relevant, especially in the context of clinical trials. This session underscores the critical importance of data cleanup and integrity as foundational to leveraging AI and ML technologies in clinical trial operations. Participants will explore strategies for ensuring high-quality data input, including standardization, validation, and cleansing practices. The session will also cover the implications of data integrity on predictive analytics, decision-making processes, and overall trial success. Through expert insights and case studies, attendees will learn how to prepare their data infrastructure for the future of digitalized clinical trials, ensuring that they can fully harness the power of AI and ML to optimize trial outcomes and operational efficiency.
Sponsor Technology Advancements: Driving Efficiency in Trial Management
Dive into the cutting-edge technologies that are transforming how sponsors manage clinical trials. This session will highlight tools and platforms that enable sponsors to oversee trial progress more effectively, from patient recruitment to data analysis. Key topics include advanced analytics for real-time decision-making, cloud-based trial management systems, and AI-driven predictive modeling. Attendees will gain insights into how sponsor technologies are improving trial oversight, reducing timelines, and enhancing collaboration with trial sites.
Florence Executive Advisory Board
TBD: A session designed for users of the Florence Site Enablement Platform
12:00pm - 1:30pm
Lunch + Networking
Enjoy a full lunch and networking.
1:30pm - 3:00pm | Workshops
Workshop: Enhancing Patient Diversity in Clinical Trials
This crucial session will focus on strategies and best practices for increasing patient diversity in clinical trials. It will address the barriers to participation for underrepresented populations, the importance of culturally competent trial design, and the impact of diversity on trial outcomes and drug efficacy across different demographics.
Site Enablement League Executive Meeting
Executive meeting of the Site Enablement League
3:00-3:30pm
Closing
Join us as we recap the key learnings from the conference and share next steps for staying involved and connected.
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