Job Description
We're looking for a Central Integrated Scientific Review Committee Lead to achieve remarkable things for patients as we positively transform healthcare.
The role involves reviewing and approving clinical documents across therapeutic areas in Development, following documents from submission to finalization, and managing meetings and documentation for completeness, consistency, and process adherence.
You'll work with the C-ISRC Chair and Co-Chair to act as project manager in the review cycle and associated activities for high-quality and efficient C-ISRC meetings.
The key outcomes include high-quality concept sheets, protocols, and clinical development plans.
You'll be responsible for managing the C-ISRC Review process, ensuring appropriate documentation and meeting management, and assisting in the development of high-quality protocols and clinical documents.
You'll also work with various systems and trackers to ensure smooth C-ISRC workflow, serve as a back-up to fellow C-ISRC Leads, and manage timely key data entry to create reports and facilitate tracking of key metrics.
Minimum qualifications include a Bachelor's degree in science, 5+ years' experience in the pharmaceutical industry, and strong knowledge of clinical drug development processes and IT systems.
This role can be based in London, UK, or Dublin, Ireland.
At Novartis, our purpose is to reimagine medicine to improve and extend people's lives, and our vision is to become the most valued and trusted medicines company in the world.
We're committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.