Beaufort CRO
Trish Landry serves as the Senior Vice President of Global Clinical Operations at Beaufort CRO, where responsibilities include building and leading collaborative teams to deliver integrated solutions across the clinical development process. With extensive experience in clinical and regulatory affairs, Trish has advanced through multiple positions at Beaufort since 2010, including Vice President of Clinical Operations and Director of Client Services. Previous roles include Independent Consultant at The Regulatory Link, Senior Consultant at M Squared Associates, Director of Regulatory Affairs at Plasma Protein Therapeutics Association, and various positions in clinical research and regulatory affairs starting from 1989. Trish holds an MBA from Loyola University Maryland and a B.S. in Biochemistry from Bowling Green State University.
Beaufort CRO
Beaufort is a global CRO built around one purpose — helping life science companies improve and save lives through the rapid development and commercialization of innovative products. Our shared interest and commitment to your success drives our entire organization to deliver best-in-class clinical trial services, regulatory strategy and planning, data and business analytics, data management and statistics, and quality services. We are: ◈ MedTech Focused - Industry-leading expertise to streamline your clinical development. ◈ IVD Specialists - Two decades of extensive diagnostic experience. ◈ Results Oriented - Guided by efficient and adaptive clinical trial management. ◈ Partnership Driven - 94% of clients rate Beaufort higher than other CROs Our experience includes: ◈ 500+ Regulatory Submissions including 510(k)s, PMAs, IDEs and CE-Marks ◈ 4,000+ Clinical Study Sites Around the Globe ◈ 1,000+ Clinical Trials Across a Wide Variety of Indications and Testing Platforms ◈ 2,600+ Clinical Professionals in Over 50 Countries See how Beaufort CRO can accelerate your medical innovation -- and put our experience to work for you.