Description
Precision Medicine Group is hiring an experienced Trial Master File TMF Lead II to support project teams across the Precision Medicine Group portfolio in Latin America. The role oversees the creation, maintenance, quality review, archival, risk management, audit support, close-out, and eTMF coordination of study Trial Master Files in accordance with GCP, FDA, ICH, and relevant SOPs. The position requires a bachelor’s degree or equivalent, at least three years of related experience, English proficiency, Microsoft Office proficiency, and experience with eTMF systems and vendors. The posting indicates a remote work arrangement.
