Database Manager állás innen: Magyarország

2025. 07. 12. | 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

2025. 07. 12. | Teljes munkaidõ | Budapest | IQVIAAnd work instructions, working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary. Review documents for completeness, consistency and accuracy, under guidance of senior staff. • Prepare site documents, reviewing for completeness and accuracy