Celina González-Colaço

Celina has over 25 years of experience in clinical trials and draws on her experience as a former regulator to support clients with their clinical trial submissions, particularly advising customers of the use and implementation of the EU Clinical Trial Regulation 536/2014.

Work experience

Prior to joining Parexel, Celina spent 12 years as a clinical trial assessor at the Spanish Agency of Medicines and Medical Devices. She also spent a further 2 years’ giving support to the EU-CTR implementation during her time at the European Medicine Agency (EMA). 

Education

Celina holds a Bachelor degree in Pharmacy from the Universidad Complutense Madrid, Spain. She also has a Diploma in Development, European register procedure and drug regulation, from the Official School of Pharmacy, and a Diploma in Public Health, Escuela Nacional de Salud (ENS) Madrid, Spain.