Offer summary
Qualifications:
Bachelor’s degree in life sciences or related field, 1 year minimum as Regulatory or SU specialist, Regulatory experience covering Belgium and Netherlands, Fluency in English and Dutch.
Key responsabilities:
- Ensure timely site activation readiness
- Prepare Clinical Trial Application Forms and submission dossiers
- Maintain communication with involved functions regarding project status
- Act as subject matter expert for site activation data points
- Keep updated on local clinical trial regulations