Offer summary
Qualifications:
Bachelor's degree in life sciences, 1+ year as Regulatory or SU specialist, Strong communication and organizational skills, Fluency in English, Preferred: Advanced degree in life sciences.
Key responsabilities:
- Ensure site activation readiness and mitigate risks
- Prepare Clinical Trial Application Forms and submission dossiers
- Maintain communication with key functions and manage essential documents
- Act as SME for site level critical path data points
- Support negotiations related to budgets and investigator contracts