Site Start Up EUCTR I
Parexel(6 days ago)
About this role
The Site Start Up EUCTR I role focuses on planning and submitting clinical trial applications within the EU, coordinating with various stakeholders to ensure compliance with regulatory standards. The position involves managing documentation, timelines, and communications to support clinical trial initiation and progress.
Required Skills
- Regulatory Compliance
- CTMS
- Project Management
- GxP
- Clinical Trials
- Documentation
- EUCTR
- IVDR
- Stakeholder Management
- Trial Management Systems
About Parexel
parexel.comFor over 35 years Parexel has been a trusted global CRO and biopharmaceutical services company. Learn more about how we can help.
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