An exciting new role with ICON's regulatory team working on high profile Pharma projects, the Regional CTA Submission Manager is accountable for leading operational submissions execution for designated CTAs, and operate as regulatory operational Subject Matter Expert for EU CTR. This role requires hands-on experience in Clinical trial applications under EU CTR.
Job listings
An exciting new role with ICON within our regulatory team working on high profile Pharma projects. The Regional CTA Submission Manager (CTA-SM) is accountable for working with contributing to business lines to lead operational submissions execution for designated CTAs and may operate as regulatory operational Subject Matter Expert for EU CTR.