About the job
What you'll do
The role involves supporting the European clinical trials environment by coordinating multinational trials and optimizing the Clinical Trials Information System. You will contribute to regulatory initiatives, perform data analysis, and facilitate stakeholder engagement across the European Medicines Regulatory Network.
What they're looking for
Candidates must hold a university degree in Life Sciences and have at least three years of professional experience in medicines regulation, pharmaceutical industry, or academic research. Proficiency in English (C1) and another EU language (B2) is required, along with current employment in the public sector.
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