Your tasks

• They independently manage the day-to-day operations of clinical trials and registries and communicate with national and international sponsors and study partners.
• They coordinate the submission of clinical studies to the ethics committee and health authority and adapt study documents in accordance with Austrian regulatory requirements.
• They perform remote monitoring and risk-based quality management and consistently follow up on open queries.
• They work closely with national testing centers as well as internal and external partners in study management.
• They proactively coordinate open issues, keep an eye on deadlines and priorities, and ensure that study processes progress reliably.
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