Regulatory Affairs Specialist — Flemish (Belgian Dutch)

Worldwide Clinical Trials seeks a Regulatory Affairs professional to lead submissions across regulatory authorities in Poland and neighboring regions. You will guide strategy, coordinate documentation, and ensure timelines align with ICH GCP and local requirements.

The ideal candidate has 3+ years in CRO regulatory roles, strong EU-CTR experience, and fluency in Flemish and English, enabling effective collaboration with multilingual teams and stakeholders.