Senior TMF Operations Specialist, EMEA/LATAM

Worldwide Clinical Trials in Mexico City seeks a TMF Records Management professional to lead TMF operations within a regulated CRO setting. You will ensure quality, compliance and timely archival of essential clinical trial documents, collaborating with global teams and Sponsor counterparts.

The role requires a degree in Life Sciences, 2–4 years’ experience in regulated environments, and strong communication to support audits and regulatory inquiries across the project lifecycle.