Coverage will include, but is not limited to:
Trial Design & Protocol Optimization
- Patient and Site Voice in Protocol Design
- Technology, Data, and AI/ML for Intelligent Trial Design
To learn more, reach out to Bridget Kotelly
Feasibility & Site Strategy
- Data-Driven Feasibility and Investigator Selection
- Tech and Collaboration to Streamline Start-Up and Reduce Site Burden
To learn more, reach out to Bridget Kotelly
Recruitment & Engagement
- Enrollment Strategy and Trial Readiness
- Access, Trust, and Participant Engagement
To learn more, reach out to Bridget Kotelly
Site Partnering, Engagement & Operations
- Building Strategic Sponsor-Site Partnerships
- Tech and Collaboration to Streamline Start-Up and Reduce Site Burden
To learn more, reach out to Bridget Kotelly
Budgeting & Resources
- Clinical Trial Budgeting, Contracting, and Payments
- Clinical Trial Resource Management and Operational Planning
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
SCOPE Biotech Forum
- Building Early-Stage Study Infrastructure
- Scaling Clinical Capabilities for Late-Stage Development
To learn more, reach out to Iris Goldman
Data
- Clinical Data Strategy
- Integrating AI into Clinical Data and Analytics
To learn more, reach out to Marina Filshtinsky
Advancing Trial Delivery
- Operational Excellence in Trial Execution
- Point-of-Care, Remote, and Decentralized Models
To learn more, reach out to Marina Filshtinsky
Digital Measures & eClinical Technologies
- Digital Endpoints and Biomarkers
- Digital Trials in a Connected Health Ecosystem
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 in Clinical Research
- Agentic AI in Clinical Research
- AI for Trial Optimization and Data Management
To learn more, reach out to Marina Filshtinsky
Quality & Monitoring
- Risk-Based Quality Management
- Central Monitoring and Signal Detection
To learn more, reach out to Iris Goldman
Safety & Pharmacovigilance
- Building a Unified Safety Ecosystem
- Next-Generation Technologies and Intelligent Signal Detection
To learn more, reach out to Iris Goldman
Biospecimen Strategy & Operations
- Modernizing Lab, Biospecimen & Data Management Operations
- Biomarker & Biospecimen Technology & Innovation
To learn more, reach out to Bridget Kotelly
Clinical Supply & Logistics
- Communication & Digitization for End-to-End Clinical Supply Management
- Clinical Supply Chain Strategies to Align Process, Products, and Patients
To learn more, reach out to Iris Goldman
Therapeutic Area Spotlights
Clinical Trial Venture, Innovation & Partnering
To learn more, reach out to Julia Boguslavsky
The deadline for priority consideration is July 21, 2026.
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.
Please note that due to limited speaking slots, preference is given to pharmaceutical and biotech companies, regulators, and those from academic/hospital centers. Additionally, as per CHI policy, a select number of vendors/consultants who provide products and services to these biopharmaceutical companies are offered opportunities for podium presentation slots based on a variety of Corporate Sponsorships.
Opportunities for Participation: