Dein persönlicher KI-Karriere-Agent
Regulatory and Start Up Specialist - Austria(m/w/x)
Site activation and regulatory document preparation for clinical trials in Austria. German fluency and 3 years' clinical research experience required. Single point of contact for studies, ensuring SOP adherence and timeline management.
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Anforderungen
- German language fluency
- Bachelor's Degree in life sciences or related field and 3 years' clinical research or relevant experience; or equivalent education, training, and experience
- In-depth knowledge of clinical systems, procedures, and corporate standards
- Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
- Knowledge of applicable regulatory requirements, local regulations, SOPs, and company's Corporate Standards
- Understanding of regulated clinical trial environment and drug development process
Aufgaben
- Perform site activation tasks according to regulations and guidelines
- Serve as Single Point of Contact (SPOC) for assigned studies
- Ensure adherence to SOPs, WIs, and project timelines
- Distribute completed documents to sites and internal team members
- Prepare and review site regulatory documents for accuracy
- Maintain internal systems and databases with project information
- Review and provide feedback on site performance metrics
- Establish and agree on project planning and timelines
- Implement monitoring measures and contingency plans
- Inform team of completed regulatory and contractual documents
- Track and follow up on document approvals and executions
- Provide local expertise during project timeline planning
- Perform quality control on documents from sites
- Communicate with sponsors on specific initiatives
Berufserfahrung
Ausbildung
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Von Nejo automatisch aufbereitet
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