Offer summary
Qualifications:
Bachelor's degree, 2+ years relevant experience, Knowledge of regulatory guidelines, Excellent oral and written communication skills, Basic medical terminology knowledge.
Key responsabilities:
- Prepare and coordinate local regulatory submissions.
- Provide local regulatory strategy advice to clients.
- Coordinate site start-up activities to align with submission timelines.
- Maintain trial status information accurately within tracking databases.
- Develop country specific patient informed consent documents.