Study Start-Up Lead: Regulatory Submissions & Site Activation

Experteer Italy is seeking a Regulatory Start-up Lead to drive efficient, compliant country-level study initiation for clinical trials. You will lead regulatory submissions, site activation strategies and vendor coordination to enable timely trial delivery, while aligning with global objectives. The role requires a Life Sciences degree and 3–4 years of experience in start-up, submissions, and CRO/vendor management, with strong ICH-GCP and EUCTR knowledge.

#J-18808-Ljbffr