- Posted 14 August 2024
- LocationDeutschland
- Job type Permanent
- DisciplineLeadership, Pharmaceuticals and Biotechnology
- ReferenceET2
Senior Director Regulatory Affairs
Job description
Associate/Senior/Executive Director
Remote/ Hybrid role
Tasks
Providing strategic regulatory guidance to project teams
Covering clinical development in the project teams
Planning and executing the global regulatory development plan
Responsible for the global agency interaction strategy
Skills
Advanced degree in life sciences, medicine or veterinary medicine
At least 10 years of experience in pharmaceutical development.
Practical experience in strategic clinical development (not clinical operations) and regulatory strategy (people management in those areas will not be sufficient).
Ideally experience across different pharmaceutical companies and/or regulatory authorities
Ability to understand and to communicate complex development scenarios
Strategic thinker, solution oriented
Ability to work independently and manage multiple tasks simultaneously under time constraints, excellent prioritisation skills
Experience with both EU and US regulatory procedures would be preferred but is not a must
Further information
Offices are in Munich/Germany
The position would support further development, however, not in terms of getting higher hierarchical managerial levels but rather in broadening the specialist skills by exposure to a multitude of different cutting-edge-of-science projects.
Position would not involve client acquisition