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--- | Your service-oriented approach is of great help to liaise with all internal and external stakeholders. Join our customer as the next reliable team member in this familial work environment. Working place is close to public transportation within Zurich area. Newly defined role: * Overseeing clinical, regulatory and technical documentation associated to clinical product candidates development
- Process documents through up their life cycle using various document sharing, reviewing and archiving platforms
- Review documents for accuracy, completeness and formal compliance
- On site presence in region Zurich is up to 4 days/week
Your profile: * Well organized, structured and detail-oriented working style
- Experience in document management such as data entry, filing or archiving
- Quality driven and ability and interest in working with different document management tools
Our customer is a R&D driven biopharmaceutical company located in Zurich. Focused on Immune Response diseases. Our client develops exciting new MAbs and partners with big pharma in clinical development. The position is defined on a temporary base and has high chance to develop into a perm role still this year. |
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