You will be responsible for regulatory strategy and Health Authority liaison activities for development products from early to late stage. In this role you will be responsible for setting the regulatory strategy for projects in oncology and immuno-oncology.
Advanced degree and minimally 10 years of relevant regulatory experience
Ideally 5 years of recent oncology experience l
Experienced strategist with a record of successful FDA interactions
Demonstrated Leadership capabilities
For further information about this position please apply.