MSI Pharma are working with a global bio-pharma to source a global safety physician for a 6 month project in the UK
The role will be working on a Phase III Rare disease study so Clinical development safety experience is a must.
- Be required to be a key contributor and assessor of the benefit-risk profile of products, including signal detection activities and risk minimisation strategies
- Provide support to the Safety Lead for Benefit Risk Team , Global Labelling Committee, Benefit Risk Board, and Patient Value Unit activities
- Contribute to the scientific analysis and review of various sources of safety data (e.g. regulatory, clinical, submission, legal, product quality)
- Medical Degree
- Minimum of 5 years of pharmacovigilance experience which must include safety surveillance/signal detection and management, benefit-risk assessment or safety risk management
Patient safety, pv, freelance. MD jobs, Global Safety,