Global Regulatory Publishing Specialist

4 weeks ago


London, Greater London, United Kingdom https:magnet.mesitemap Full time
Global Regulatory Publishing Specialist

We are seeking a skilled Global Regulatory Publishing Specialist to join our Regulatory Operations Team. As a key member of our team, you will be responsible for publishing, verifying, and dispatching clinical documents and submission dossiers worldwide.

Key responsibilities include:

  • Preparing and publishing clinical documents and submission dossiers in compliance with worldwide health authority requirements
  • Verifying and validating clinical documents and submission dossiers to ensure accuracy and quality
  • Dispatching and archiving clinical documents and submission dossiers in a timely and efficient manner

Requirements:

  • Bachelor's degree in life sciences or relevant discipline
  • Clinical report and global submission dossier publishing/compilation experience in the pharmaceutical or related industry
  • Working knowledge of electronic clinical document publishing standards/formats, electronic and global regulatory submission publishing standards/formats

As a Global Regulatory Publishing Specialist, you will have the opportunity to work with a talented team of professionals who are passionate about delivering high-quality results. If you are a detail-oriented and organized individual with excellent communication skills, we encourage you to apply for this exciting opportunity.

Commitment to Diversity & Inclusion

Novartis is committed to building an outstanding, inclusive work environment and diverse team's representative of the patients and communities we serve.



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