Global Regulatory Affairs Lead – Trials & Submissions

IQVIA in Mexico City is seeking a Regulatory Team Lead to oversee complex global studies, ensuring quality regulatory documentation and strategic client engagement. You will lead the drafting and review of core regulatory study documents and work with Competent Authorities across multiple regions.

The role requires a Bachelor’s or Master’s degree in Life Sciences and 3–4 years of relevant experience. Ideal candidates will have a strong understanding of clinical trial regulations and excellent communication abilities.