Senior Medical Writer overseeing high - quality clinical and regulatory documents at Ipsen, a biopharmaceutical company. Leading cross - functional teams and contributing to regulatory strategy while ensuring compliance and innovation in medical writing practices.
About the role
- Medical Writer I role focusing on document management within Veeva systems for clinical projects. Supporting compliance and adherence to GxP guidelines while collaborating with stakeholders.
Responsibilities
- Support accurate and compliant document filing within Veeva RIM
- Perform eTMF filing activities while adhering to GxP guidelines
- Manage document handling activities within Veeva
- Ensure documents meet quality and integrity standards
- Categorize documents systematically for retrieval
Requirements
- 1–2 years of experience in ETMF filing and Document management systems
- Experience in Filing documents based on Versions, Metadata and Filing structure
- Experience of Veeva (Viva) RIM / Veeva Clinical
- Good understanding of GxP guidelines
- Excellent communication skills in English
Benefits
- Career development and progression
- Supportive and engaged line management
- Technical and therapeutic area training
- Peer recognition and total rewards program
- Total Self culture promoting authenticity
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
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