Regulatory Submissions Associate (Clinical Trials)

FTMEX Fortrea Clinical Development Mexico S.DeR.L.DeC.V. seeks a Regulatory Submissions Associate to support investigator sites and regulatory documents, ensuring timely EC/IRB/Third‑party approvals with project management.

You will assist with preparing, submitting, and obtaining approvals, liaise with vendors, and maintain audit-ready study files in line with ICH/GCP and local regulations. 0–2 years experience preferred; life sciences degree required.