Clinical Report Specialist

hace 1 semana


Barcelona, Barcelona, España Bayer A tiempo completo

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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