Global Regulatory Publishing Specialist
4 weeks ago
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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