Pharma R&D Specialist
hace 2 semanas
Bayer is a global leader in the life sciences, and we're committed to making a positive impact on people's lives. Our Preclinical Development team is responsible for creating, preparing, and processing non-clinical toxicology and DMPK reports for authority submissions. We're looking for a talented individual to join our team as a Junior Non-Clinical Report Specialist.
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
- Excellent skills in Microsoft Office Word and Adobe Acrobat Pro DC
- Familiarity with Document Management System (DMS) BRAVE and compilation tools (docuBridge)
- Very good verbal and written English skills, with German skills a plus
- Basic knowledge of and experience with Good Laboratory Practice (GLP)
Bayer is a company that values diversity, equity, and inclusion. We're committed to creating a workplace where everyone feels welcome and valued. As a Junior Non-Clinical Report Specialist, you'll have the opportunity to work with a talented team of professionals who are passionate about making a difference. You'll also have access to ongoing training and development opportunities to help you grow in your career.
We're an equal opportunities employer and welcome applications from all individuals, regardless of race, national origin, gender, age, physical characteristics, social origin, disability, union membership, religion, family status, pregnancy, sexual orientation, gender identity, gender expression, or any unlawful criterion under applicable law.
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