Clinical Trial Associate

17 ore fa


Turbigo, Italia Planet Pharma A tempo pieno

Planet Pharma is seeking a Clinical Trial Associate (CTA) to provide key operational and administrative support to a global Clinical team. This role plays an important part in maintaining quality systems, training compliance, documentation and clinical platforms, helping to ensure efficient and compliant clinical development activities. Key Responsibilities Maintain and regularly update SOP inventories, training matrices and compliance documentation. Coordinate, assign, track and document training activities in line with regulatory and internal requirements. Support clinical administrative processes including CV management, onboarding documentation, vendor tracking and organizational charts. Manage system access and user coordination for platforms such as eTMF, Veeva QDocs and DocuSign, working closely with IT and internal stakeholders. Assist with the planning and coordination of internal and external meetings, ensuring logistics, materials and documentation are prepared. Serve as first-line support for basic system and access-related issues, ensuring clear and effective communication with relevant teams. Qualifications & Skills Bachelor’s degree in a scientific, pharmaceutical, biomedical or related discipline (or equivalent relevant experience). Strong working knowledge of Microsoft Office (Excel, Word, PowerPoint, Outlook and SharePoint). Highly organized with strong attention to detail and the ability to manage multiple priorities in a fast-paced environment. Fluency in English (written and spoken) is required. Fluency in Italian is required. Preferred experience within clinical research, pharmaceutical, or biotech environments, with familiarity in systems such as SAP SuccessFactors, eTMF, DocuSign and Veeva QDocs and an understanding of 21 CFR Part 11. #J-18808-Ljbffr



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