Clinical Report Specialist
hace 1 semana
Job Summary
We are seeking a skilled Clinical Report Specialist to join our Preclinical Development team at Bayer. As a key member of our team, you will be responsible for the technical preparation and processing of non-clinical toxicology and DMPK reports for authority submissions.
Key Responsibilities
- Technical preparation of non-clinical reports for eCTD readiness in Document Management (DMS) System BRAVE
- Processing and compilation of regulatory submission relevant non-clinical reports in DMS BRAVE
- Collaboration with the ED Documentation Group to ensure seamless communication and onboarding
Requirements
- Excellent technical skills in Document Management systems
- Good team player with excellent verbal and written English skills
- Very good verbal and written German skills would be an asset
- Basic knowledge of and experience with Good Laboratory Practice (GLP)
About Bayer
Bayer is a global leader in the life science industry, committed to making a positive impact on people's lives. We are a community of brilliant and diverse minds working together to tackle the world's biggest challenges. If you're passionate about making a difference, we want to hear from you.
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