Senior Report Specialist
hace 4 días
Job Summary
We are seeking a skilled Senior Report Specialist to join our team in Preclinical Development. The successful candidate 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 System BRAVE
- Processing and compilation of regulatory submission relevant non-clinical reports in DMS BRAVE
Requirements
- Excellent technical skills in Document Management systems
- Good team player with ability to work in a structured manner according to regulations
- Independent allocation and completion of workload and organization of daily work
- Ability to independently solve problems in the event of deviations from the standard process
Additional Information
Bayer is an equal opportunities employer and welcomes applications from all individuals. We are committed to treating all applicants fairly and avoiding discrimination.
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