About me
Teresa has 15+ years of industry experience in drug development—a majority in a contract research organization—spanning regulatory affairs, market access, and medical writing. At Fortrea, Teresa’s focus is as a Clinical Regulatory Strategist where she provides guidance and input into global development programs across drug classes and therapeutic areas, aiding in the achievement of key regulatory and commercial milestones for sponsors. Her remit and expertise also includes diversity action plans; of which, Teresa and her counterparts have championed dozens of plans since 2023, partnering with both large and small-sized sponsor organizations to support adequate representation in clinical trials.
