About this role
Senior Clinical Research Associate - Poland - 0.25FTE at Propharmagroup. Location: Leiden or Netherlands or Poland. Role: conducting monitoring, reviewing documents, communicating stakeholders Requirements: Clinical monitoring for investigational sites per protocol, GCP and ICH; EDC/CTMS/IVRS/eTMF experience; Microsoft Office proficiency; bachelor’s degree or equivalent; >5 years CRA experience. Category: Research and Development (R&D) Seniority: Senior Level Tools: Microsoft Outlook, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, EDC, CTMS, IVRS, eTMF Commitment: Part Time Workplace: Hybrid Languages: English