About
Ed Lewis is Director of Clinical Trial Supplies at IQVIA, where he leads strategic clinical supply chain solutions supporting global pharmaceutical, biotechnology, and emerging sponsor organizations. With more than 25 years of experience across FMCG, healthcare, and pharmaceutical sectors, including over 20 years dedicated to clinical research, Ed brings extensive expertise in clinical trial supplies, project and supply chain management, drug importation and exportation, vendor management, and global project leadership. A founding leader of IQVIA's Clinical Trial Supplies organization, Ed has played a key role in developing and expanding supply chain services that support Phase I to Phase IV clinical studies worldwide. His experience spans sourcing, clinical packaging and labeling, cold chain logistics, global distribution strategies, named patient programs, and complex supply chain solutions across diverse regulatory environments. Throughout his career, Ed has partnered with both large pharmaceutical companies and emerging biopharma organizations, helping sponsors navigate increasingly complex global supply challenges while maintaining patient focus, quality, and compliance. His therapeutic area experience includes oncology, immunology, internal medicine, and CNS disorders. Ed holds a Master of Science in Clinical Research with Distinction from Cardiff University and is a recognized industry leader in clinical trial supply strategy, operational excellence, and innovative approaches to supporting global clinical development programs.
Contact
| Location | Reading, Other, United Kingdom |
| Company | IQVIA |
| Position | Director, CTS |
| ed.lewis@iqvia.com |
Industry Related Information
| Membership Segmentation | Service Provider |
| Areas of Expertise |
Packaging / Labelling Manufacturing Clinical Supplies Management Logistics / Import & Export Procurement / Sourcing |
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