Paul Gillard

Background

About Paul Gillard

I am highly skilled in pharmaceutical product development with extensive clinical, regulatory, and pharmacovigilance experience, and a proven track record of leadership and people management. I am an alumnus of the University of Brussels, where I earned my medical degree in 1993 and my internal medicine degree in 1998. Over the past 25 years, I have dedicated myself to the clinical development of drugs in oncology, critical care, and infectious diseases, including prophylactic vaccines.I have successfully guided clinical development plans from Phase I through Phase IV, leveraging a comprehensive understanding of diverse biopharmaceutical technologies and addressing various indications and target populations. My professional journey includes extensive collaboration with regulatory bodies such as the US FDA, EMA, and PMDA, where I have navigated the complexities of regulatory filings and licensure submissions. My expertise encompasses critical analysis, creative problem solving, and out-of-the-box thinking, which I apply to complex clinical scenarios. I excel in brainstorming balanced with timely decision-making, ensuring decisions are made by balancing risks and mitigation strategies. Additionally, I have demonstrated strong leadership and people management skills, effectively leading teams and managing personnel to achieve project goals and drive innovation in clinical development.