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Kathleen Port is a Clinical Trials Professional with over 20 years of experience in managing data management activities, including expertise in SDTM deliveries at GSK, where they currently serve as a Principal Project Lead. Previously, they held various roles at notable companies such as Pfizer and Roche Pharmaceuticals, leading studies across multiple therapeutic areas, from Phase I to IV. Kathleen has been recognized for their technical knowledge as a Subject Matter Expert in several systems and has consistently delivered high-quality data in complex environments. They earned a degree in Pharmacology from the University of Bristol.