Offer summary
Qualifications:
Bachelor’s degree in life sciences or scientific discipline, At least 8 years of experience in clinical regulatory affairs, 3 years in a management role, Knowledge of regulatory processes and Health Authorities, Fluency in English; additional languages a plus.
Key responsabilities:
- Oversee Regulatory Affairs activities and teams
- Lead global regulatory activities for trials
- Manage performance reviews and team development
- Serve as main contact for regulatory issues
- Evaluate budgets and participate in proposal requests