EU CTR Submissions Specialist — CTIS Expert

A mid-sized biotechnology company in Switzerland is seeking an EU CTR Submission Specialist responsible for managing regulatory submissions for clinical trials in compliance with EU regulations. This role involves preparing applications, managing modifications, and coordinating with various departments to ensure compliance. The ideal candidate holds a relevant Bachelor's degree and has 1-3 years of experience in regulatory operations, alongside strong organizational and communication skills.

Join a team committed to changing lives through innovative medicines.
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