Address
Form of work
SalaryLocation:
Home working – 6 days a month in the office
Responsibilities:
- Lead safety evaluation for designated products including signal detection and analysis and safety reporting
- Provide safety expertise to international project teams
- Lead the safety aspects of clinical trials – being involved in protocol design, IBs and data review
- Maintain risk management plans
- Lead the production of safety information
- Proactively manage global safety for a specific product / group of projects
- Work in a highly cross-functional and collaborative environment – clinical, regulatory, BD, medical affairs etc.
Your Background:
- Qualified Medical Doctor with GMC or similar registration
- Hold previous experience as a pharmacovigilance physician / Drug Safety Physician
- Previous experience in oncology would be advantageous
- Excellent communication skills and the ability to work in a highly collaborative and cross-functional environment
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 56436 in all correspondence.
