Nancy is the founder and President of the Board at Ad Hoc Clinical, a contract research organization (CRO) that specializes in study startup and monitoring clinical trials across Europe. Prior to establishing her own company, Nancy developed extensive expertise in Clinical Operations covering various therapeutic areas. Since 1996, she has gained experience in both the pharmaceutical industry and the CRO sector. As a Clinical Research Expert, Nancy holds a Master's degree in Strategy and Organization and is also a trained Data Privacy Officer. In addition to her role at Ad Hoc Clinical, Nancy serves as a Board member for Biovia, the health innovation cluster in Flanders, Belgium. Biovia is an industry-led membership group encompassing medical biotech, medtech, digital health, agtech, and industrial biotech. Nancy contributes her knowledge as an expert in European Regulatory and Clinical Affairs, regularly providing training on these subjects to clients, universities, and her own team. She is fluent in Dutch, French, English, and Spanish. Her true passion lies in coaching clinical trial professionals—both beginners and experienced experts—towards excellence through customized training modules: · Guiding CRAs from study startup through publication · Co-monitoring and personalized coaching · Organizing and initiating clinical trials or investigations in different EU countries · Solving data privacy challenges