TRABAJO REGULATORY AFFAIRS STUDY START BARCELONA, BARCELONA

Managing and maintaining comprehensive and accurate records of regulatory submissions, approvals, and correspondence providing guidance and support to study teams...

This is what you will do: the clinical study administrator (csa) assists in the coordination of study activities from the start up to execution and close out within...

Supports the review of the clinical study report external: supports development of investigator/site relationships to support site selection and study start up activities...

Desirable skills/experience: broad experience across multiple therapeutic areas and across all phases of clinical trials experience in regulatory submissions and...