LATAM Regulatory Affairs Associate: Submissions

Worldwide Clinical Trials in Mexico City seeks a Regulatory Affairs Associate to support the regulatory submission process for global clinical trials. The role includes coordinating translations, packing submissions, performing QC checks, and liaising with Finance.

The ideal candidate should have at least 2 years of supporting experience, preferably in a CRO or pharmaceutical environment, and must possess excellent communication skills. A Bachelor’s degree is preferred, along with fluency in the local language and working knowledge of English.