EU CTR Submission Specialist - Warszawa

Position Summary The EU CTR Submission Specialist is responsible for planning, preparing, managing, and maintaining regulatory submissions for clinical trials in compliance with EU Clinical Trial Regulation (EU CTR 536/2014) via the Clinical Trials Information System (CTIS). This role covers the entire lifecycle of a clinical trial, from initial application through substantial modifications to end-of-study reporting and public disclosure deliverables. Key Responsibilities 1. Regulatory Submissi… Zobacz pełną ofertę