Regulatory Trials Associate — EU & Global Submissions

IQVIA in Mexico City is looking for a Clinical Trial Regulatory Manager to manage regulatory projects, from straightforward tasks to complex ones with guidance. The ideal candidate should hold a Bachelor's Degree in Lifescience and have 1-2 years of relevant experience, particularly with EU CTIS. Responsibilities include preparing clinical trial submission dossiers and providing guidance to internal and external clients. The role requires strong interpersonal communication skills, attention to detail, and the ability to manage multiple projects simultaneously.