Clinical Trials Start-Up Specialist
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Fortrea in Brussels seeks a Regulatory Submissions Specialist to support site activities, collect essential documents, and ensure timely regulatory submissions across EU countries. You will work with senior staff to compile, prepare, submit, and obtain approvals from IRB/IEC/Regulatory Authorities, liaise with vendors, and ensure compliance with ICH/GCP guidelines and local laws.
Minimum degree in life sciences with 0–2+ years of experience; CTIS familiarity and strong attention to detail are