Cambridge Healthtech Institute’s 16th Annual

SCOPE—Summit for Clinical Ops Executives

Driving Innovation in Clinical Trials & Digital Health

February 3-6, 2025

Clinical trials, digital health, and clinical research are essential for advancing medical knowledge, improving patient care, and developing new treatments and therapies for the patients who need them. Execution of this vital work requires collaboration, innovation, and strategic decision-making. Now in its 16th year of fostering these joint efforts to be inclusive of all stakeholders, SCOPE Summit 2025 will take place February 3-6, 2025, in Orlando, FL, at the Rosen Shingle Creek. Over four stimulating days of in-depth discussions and networking, SCOPE features 30 different conferences (3 new), a bustling exhibit hall with 300+ companies (45 more than last year), 3 plenary keynote sessions, the 9th annual Participant Engagement Awards, the 2nd annual Site Innovation Award, special cross-department panels, multiple receptions, the 4th annual Master of Clinical Research golf tournament, a morning Fun Run, and an exclusive Venture/Partnering event with Start-Up Pitch Contest. SCOPE keeps gaining momentum (14% YoY Growth last year alone!). At the request of our attendees, we have extended the coverage in 2025 on Patient-Centric Trial Design, Site Engagement, Recruitment, Generative AI, Small Biopharma Strategies, and other key topics. The programming focuses on advances and innovative solutions in all aspects of clinical trial innovation, planning, management, operations, and investment. SCOPE welcomes more than 4,000 attendees and 1,200 different organizations from 30 countries, in clinical operations, innovation, and digital health, and we want you and your company to join the community!

SUBMIT YOUR SPEAKING PROPOSAL FOR THE TOPICS BELOW

The deadline for priority consideration is August 2, 2024

Coverage will include, but is not limited to:

Patient-Centric Trial Design & Inclusive Research

• Patient Voice in Trial Design and Protocol Development
• Developing and Executing Effective Diversity Plans

To learn more, reach out to Bridget Kotelly

Feasibility & Study Start-Up

• Data-Informed Feasibility and Investigator Selection
• Tech and Collaboration to Streamline Start-Up and Reduce Operational Burden

To learn more, reach out to Bridget Kotelly

Recruitment & Engagement

• Enrollment Planning and Patient Recruitment
• Patient Engagement and Retention through Communities and Technology

To learn more, reach out to Bridget Kotelly

Site Engagement & Enablement

• Collaborative Strategies to Improve Trial Execution
• Tech and Collaboration to Streamline Start-Up and Reduce Operational Burden

To learn more, reach out to Bridget Kotelly

Budgeting & Resources

• Clinical Trial Forecasting, Budgeting and Contracting
• Resource Management and Capacity Planning for Clinical Trials

To learn more, reach out to Kaitlin Searfoss Kelleher

Outsourcing

• Mastering an Outsourcing Strategy
• Relationship and Alliance Management in Outsourced Clinical Trials

To learn more, reach out to Kaitlin Searfoss Kelleher

Small Biopharma Strategies

• Partner Selection and Trial Design
• Vendor Oversight & Resource Management

To learn more, reach out to Eileen Murphy

Data

• Clinical Data Strategy and Analytics
• Data Science, ML, and AI

To learn more, reach out to Marina Filshtinsky

Decentralized & Hybrid

• Decentralized and Hybrid Trials
• DCTs and Clinical Innovation

To learn more, reach out to Marina Filshtinsky

Digital Health Technologies

• Digital Biomarkers and End Points in Clinical Trials
• Digital Measurements Implementation at Scale

To learn more, reach out to Marina Filshtinsky

Real World Evidence

• Accessing and Generating RWD
• Leveraging RWD for Clinical Research

To learn more, reach out to Marina Filshtinsky

AI for Clinical Trials

• Generative AI in Clinical Research
• AI for Trial Optimization

To learn more, reach out to Marina Filshtinsky

Quality & Monitoring

• Risk-Based Quality Management
• Central and Remote Monitoring

To learn more, reach out to Iris Goldman

Biomarkers & Precision Medicine Trials

• Modernizing Lab, Biomarker & Data Management Operations
• Biomarker & Biospecimen Technology & Innovation

To learn more, reach out to Bridget Kotelly

Clinical Supply & Logistics

• Data Technology for End-to-End Clinical Supply Management
• Clinical Supply Chain Strategies to Align Process, Products and Patients

To learn more, reach out to Mary Ann Brown

Clinical Trial Venture, Innovation & Partnering

To learn more, reach out to Eileen Murphy

The deadline for priority consideration is August 2, 2024.

All proposals are subject to review by session chairpersons and/or the Scientific Advisory Committee to ensure the overall quality of the conference program. Additionally, as per Cambridge Healthtech Institute’s policy, a select number of vendors and consultants who provide products and services will be offered opportunities for podium presentation slots based on a variety of Corporate Sponsorships.

Opportunities for Participation:

• To submit a podium presentation, please click here.
• To become a sponsor, click here.
• To sign up to attend, click here.

For more details on the conference, please contact:

For sponsorship information, please contact:

For media and association partnerships, please contact: