Regulatory Affairs Manager IVDR

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

**Regulatory Affairs Manager IVDR -** Homebased in the UK/Europe

The role will support clinical trial application submission activities with a dedicated focus on IVDR-related processes, particularly for studies involving companion diagnostics or combined clinical trial/IVDR submissions.

**What You Will Do:**

The role will support clinical trial application submission activities with a dedicated focus on IVDR-related processes, particularly for studies involving companion diagnostics or combined clinical trial/IVDR submissions.

**Your Profile:**

+ Deep understanding of IVDR-related processes and their impact on clinical trial submissions...