Rebeca Zorrilla

Rebeca Zorrilla has worked in the clinical research and development field since 2004. From 2004 to 2006, they were a Research Assistant at the University of Vigo, where they were responsible for Toxicology Research within the Analytical Department. Rebeca then worked as a Study Director/Senior Scientist at ESG UK from 2006 to 2011, where they gained experience in planning, coordination and delivery of GLP and GCP studies, including study protocols and technical reports writing. From 2011 to 2018, they worked at NovImmune as a Project Manager and Senior Project Coordinator, where they were responsible for assisting project teams to define objectives, strategy, resources and costs to ensure delivery of project milestones according to agreed timelines and budget. Most recently, they have been working at iOnctura as a Clinical Program Lead since 2018, where they are responsible for assisting internal and external project teams in the conduct of clinical trials, preparing project plans, managing project timelines and budget.

Rebeca Zorrilla completed an Advanced Master of Management of Biotechnology companies at Grenoble Ecole de Management from 2010 to 2011 in the field of Biotechnology. Additionally, they obtained a MSc in Chemistry from Universidade de Vigo between 1996 and 2002, specializing in Analytical Chemistry.