Clinical Report Specialist

hace 2 semanas


Barcelona, Barcelona, España Bayer A tiempo completo
Join Bayer's Team of Experts

Bayer is a global leader in the life sciences, and we're committed to making a positive impact on people's lives. As a Junior Non-Clinical Report Specialist, you'll play a critical role in supporting our Preclinical Development team in creating and processing non-clinical toxicology and DMPK reports for regulatory submissions.

Key Responsibilities:
  • Technical preparation of non-clinical reports for eCTD readiness in the Document Management System (DMS) 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 and Microsoft Office Word
  • Familiarity with Adobe Acrobat Pro DC 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)
What We Offer:

Bayer is committed to creating a diverse and inclusive work environment that fosters growth, innovation, and collaboration. As a Junior Non-Clinical Report Specialist, you'll have the opportunity to work with a talented team of experts, develop your skills, and contribute to the development of life-changing medicines and solutions.

We 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. We're committed to treating all applicants fairly and avoiding discrimination.



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