Tessa Beecher-Jones, BSc

Mrs. Beecher-Jones is a pharmacologist with over 26 years’ experience in international clinical R&D, leading or supporting the development of product candidate to Proof of Concept, NDA, sNDA, MAA, or out-licensing. She gained her expertise in both operational and senior leadership roles in US and European biotech and start-up companies, as well as medium to large pharma, CROs and her own successful consulting business.

Mrs. Beecher-Jones has both strategic and hands-on operational leadership expertise from the project management of a single clinical project to full programme management of global cross functional and multi-disciplinary development teams.  She has a passion for proof of concept and orphan disease studies, designing and delivering optimal, scientifically driven studies to answer the key questions needed to bring new treatments to patients in areas of unmet need. As an integral part of this Mrs. Beecher-Jones builds and maintains relationships with the Key Opinion leaders, running Advisory Board meetings, and engaging with Patient Advocacy groups.

Mrs. Beecher-Jones has a variety of indication experience including pain, arthritis, neurology, immunology and more recently has been focussed in hepatology and gastroenterology, bile acid therapeutics and diseases of high unmet medical need. Further details of Mrs. Beecher-Jones’s career and indication experience are found in her LinkedIn profile here.

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