Privacy in Clinical Trials with Jim Schneider

Episode notes

Clinical trials pose unique privacy challenges where scientific integrity, ethics, and compliance intersect. In this episode, Jim Schneider of Immunome shares practical insights from over 15 years of biopharma privacy leadership. From untangling the complexities of GDPR and HIPAA to tackling cross-border data transfers and handling future use of trial data, Jim explains how privacy professionals embed privacy into clinical research without slowing down innovation. This episode offers foundational insights for privacy professionals and business leaders seeking to understand the basics of compliance in clinical trials and how it can drive business growth while navigating legal hurdles. What You'll Learn: How to balance GDPR and GCP in clinical trial consent Why HIPAA often doesn't apply to clinical trial sponsors How to manage data subject rights while maintaining trial integrity Practical steps for handling cross-border data transfers in clinical research Key insights on the future use of clinical trial data And so much more! Jim Schneider is the Senior Director, Counsel of Compliance and Data Privacy at Immunome, a clinical-stage oncology company.

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