Offer summary
Qualifications:
Minimum of 3 years in clinical trials, Proven ability to lead cross-functional teams, Experience in oncology clinical trials, Knowledge of GCP/ICH guidelines.Key responsabilities:
- Manage country level components of clinical studies
- Ensure compliance with procedural documents and regulations
- Prepare and maintain study budgets
- Optimize performance of Local Study Teams
- Submit necessary documents to EC/IRB