Job SummaryPerforms assigned activities within the country that lead to start-up of investigative sites in all phases of clinical trials. Responsible for delivery with oversight from Line Manager in areas such as investigator site contracts, ethics and
CDMX What You Will Do Trial Documentation & eTMF Management Oversee clinical trial documentation, including CTA packages for Health Authority (HA) and Ethics Committee (EC) submissions. Maintain and ensure compliance of the electronic Trial Master File