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.

You will:

• 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)

Experience requirements;

• 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

Key words;

Patient safety, pv, freelance. MD jobs, Global Safety,