Top Job | 2025. 07. 25. | Teljes munkaidõ | Budapest | IQVIAFor clinical trials with medical devices (e.g. ICH-GCP, ISO 141552020, MDR, FDA 21 CFR) under supervision of the Regulatory & Start-up Manager. Main responsibilities Search and verifies NCA/EC/IRB submission requirements. Drafts NCA/EC/RIB submission documents (e.g. application form, ICF, …). Prepares NCA/EC
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