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From Chaos to Clarity: A Founder’s View from 30 Years in Drug Development
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Past Recordings

How Patient Advocacy Groups Are Rewriting the Clinical Trial Playbook
The Secret Sauce Behind High-Enrolling PIs
Challenges to Making Go/No-Go Decisions in Clinical Trials
What It Really Takes to Become the Sponsor of Choice
Where the Data Starts: Rebuilding Sponsor-Site Alignment on Source
Translating R3 Data Governance & Oversight into Practice
Tackling the Biggest Challenges in Clinical Pharmacology in Drug Development
Adapting Digital Solutions to Site Workflows
Reimagining Site Contracting
Pediatric Patient Engagement
Sponsor-Provided Technology: Challenges to Site Adoption
Clinical Trial Oversight: Top Sponsor Misconceptions
Insights Every Sponsor Must Know About Sites
How Sponsors Turn Vendors Into Partners
Navigating the Transition From Early to Late State Development
What Is Source Data?
Patient Burden in Clinical Trials
Queries, Queries, Queries
Biological Samples in Clinical Trials
Hear From Site Coordinators
Challenges With Biological Samples
Challenges With Sample Tracking in Clinical Trials
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