Clinical Development Quality Lead
Vor 5 Tagen
**Clinical Development Quality Lead**
You will lead the implementation of the quality startegy within Clinical Development.
**Responsibilities**
- Managing document & data accuracy (eCTD Module 5)
- CRO/Vendor selection and qualification process
- Collaborate with the Clinical Trial Manager and Study Teams
- Compliance oversight on clinical quality
- Reviewing clinical study documents to ensure cross-document consistency
- Lead / contribute to compound-specific Regulatory Authority Inspections / Due Diligence Activities
- Build collaborative working relationships and ensure adequate communication within the compound-specific study team and cross-functional Quality peers, assist in driving change to build a culture of compliance throughout the Clinical Development organization
- Provide Audit / CAPA support
**Requirements**:
- University Degree in Sciences
- Min 6 years of experience in the clinical setting in the pharmaceutical/biotech industry
- Min 3 years within Clinical Quality Management System & Compliance
- Excellence knowledge of GCP and experience in managing and conducting GCP audits
- Exoerience in QA vendors oversight
- Fluent in English, French an asset
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