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Job Description
Central Integrated Scientific Review Committee Lead: Collaborate with the C-ISRC Chair and Co-Chair to manage the review process for 100+ clinical documents annually. Key responsibilities include ensuring proper documentation and meeting management, developing high-quality protocols, and working with various systems to ensure smooth workflow.
Key skills and qualifications include:
- Minimum Bachelor’s degree in science
- 5+ years of experience in the pharmaceutical industry
- Strong knowledge of clinical drug development process
- Excellent interpersonal, communication, and meeting management skills
- Advanced medical/scientific writing and communication skills
Join Novartis to reimagine medicine and improve people’s lives. Benefits include a commitment to diversity and inclusion, a talent community, and a comprehensive handbook.
Company: Novartis Pharmaceuticals UK Ltd.