QA GCP
Pubblicato il 12-09-2026 - Fondazione Telethon in Muggiò
Fondazione Telethon ETS (FT) is committed to developing therapeutic options for patients affected by rare genetic disorders. FT pipeline consists in various programs at different development stages (from pre-clinical to commercial). For such programs, Telethon is responsible, among others, to act as Sponsor in the conduction of clinical trials to assess safety and efficacy of Advanced Therapy Medicinal Products and as Marketing Authorization Holder in guaranteeing post-marketing pharmacovigilance.
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The primary purpose of this role is to work closely with Clinical Operations and Pharmacovigilance functions to support compliance with GCP/GVP, applicable regulations, and the internal Quality Management System. Key responsibilities also include service provider oversight, auditing, study risk management, and contributing to the maintenance of the FT Quality Management System (including deviation management, CAPAs, procedures, and change control).
The Quality Assurance Associate will interact closely with the other QA functions, the Clinical Development and Operations, Pharmacovigilance and Regulatory Affairs Units, and with clinical centers and external service providers.
RESPONSABILITIES:
- Guarantee GCP compliance throughout the management of clinical trial activities and study documents revision, both for interventional and non-interventional studies, in close collaboration with the Clinical Development and Operations Unit
- Guarantee GVP compliance for commercial products, in close collaboration with the Pharmacovigilance Unit
- Perform, alone or in cooperation with SMEs and/or external consultants, qualification audits to service providers and study audits to clinical sites and TMF
- Implement and maintain the study risk matrix in coordination with the other FT units.
- Manage quality records such as external and internal non-compli