Ilaria Marcodoppido

Background

About Ilaria Marcodoppido

Highly experienced clinical research professional with over 38 years in the pharmaceutical industry. Currently serving as a Senior Initiation Clinical Research Associate at Parexel International in Milan, Italy, she has held various roles of increasing responsibility throughout her career. Her expertise spans clinical trial management, regulatory affairs, pharmacovigilance, and project coordination. In her current role, Marcodoppido is responsible for building relationships with investigators and site staff, managing regulatory documentation, and overseeing the initiation and activation of clinical trial sites. She demonstrates strong leadership skills by mentoring new team members and providing support across departments. Her deep understanding of Italian regulatory requirements has made her a valuable resource for colleagues and sponsors alike. Marcodoppido's career progression showcases her adaptability and commitment to the field. She has worked for several prominent pharmaceutical companies, including Eurand, Pharmacia, Monsanto, Searle Farmaceutici, and SmithKline Beecham. Her roles have encompassed diverse responsibilities, from clinical trial administration and safety monitoring to product management and general management assistance. Her educational background includes diplomas in interpreting and translating for both French and English, as well as a scientific high school diploma. This linguistic proficiency has undoubtedly contributed to her success in navigating the international aspects of clinical research. Marcodoppido is fluent in Italian, English, and French, which enhances her ability to work effectively in multinational settings. Throughout her career, Marcodoppido has demonstrated a commitment to quality, compliance, and continuous improvement. Her involvement in task forces and industry associations highlights her dedication to advancing the field of clinical research and contributing to the development of more efficient processes.