Key skills
Communication
About this role
Role Overview
- Supports Global Study Managers (GSMs) and other SOMs in study management
- Manages study startup process and oversees pCRO
- Liaises with regulatory colleagues in country
- Ensures compliance with local regulations and timely communication
Requirements
- Bachelor's of Science or Bachelor's of Arts degree
- Minimum 5 years of relevant operational clinical trial experience required
- Master’s of Science or Master’s of Business Administration degree with a minimum 3 years of relevant operational clinical trial experience required
- Experience in study and quality management
- Knowledge of clinical trial methodology
- Demonstrated clinical research experience and/or study management/startup project manager experience
Benefits
- Health insurance
- Flexible work arrangements
- Professional development