Senior Report Specialist
hace 6 días
At Bayer, we're driven to solve the world's toughest challenges and strive for a world where health for all and hunger for none is no longer a dream, but a real possibility.
The Report Management team in Preclinical Development supports the technical creation, preparation, and processing of non-clinical toxicology and DMPK reports for authority submissions.
The team ensures eCTD readiness and compliance with regulatory requirements.
We're looking for a skilled professional with excellent technical skills in Document Management systems and the ability to work in a team.
Key Responsibilities:
- Technical preparation of non-clinical reports for eCTD readiness in Document Management
- Processing and compilation of regulatory submission relevant non-clinical reports in DMS BRAVE
Requirements:
- Excellent skills in Microsoft Office Word
- Excellent skills in Adobe Acrobat Pro DC
- Familiarity with the Document Management System (DMS) BRAVE
- Very good verbal and written English skills
- Very good verbal and written German skills would be helpful
What We Offer:
At Bayer, you'll have the opportunity to work on challenging projects and contribute to our mission of making a difference in people's lives.
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