Cedric Marchand

VP, Global Head of Statistical Programming

Cedric brings over 25 years of extensive experience in the pharmaceutical industry. Throughout his career, he has worked as Lead statistical programmer on numerous clinical trials spanning phases I to IV, and has been involved in a wide range of activities including integrated summaries of efficacy and safety, CDISC e-Submission, drug development lifecycle management, exploratory analyses, responses to regulatory agencies, and publication support.

With a rich background in both CRO and pharmaceutical companies, Cedric has amassed significant experience in project management and people management since 2009. He manages globally distributed remote teams, fostering collaboration and communication across different time zones and cultures, ensuring that projects are completed to high standards of quality and achieving organizational goals and initiatives.