About this role
Role Overview
- Responsible for study and regional or specific country level activities from study startup through conduct and study close
- Serves as leader of the local study team on one or more studies
- Oversees the preferred Contract Research Organization and/or Country Trial Manager/Site Care Partner for assigned studies
- Liaises with SCP, Lead SCP, and regulatory colleagues in country to agree on submission strategy to Health Authorities and Ethics Committees
- Provides country level input on startup and recruitment milestones during planning
- Collaborates with accountable roles to identify and manage deviations and risks in study startup and execution
Requirements
- Bachelor’s of Science or Bachelor’s of Arts degree
- Minimum 7 years of relevant operational clinical trial experience required
- Master’s of Science or Master’s of Business Administration degree with a minimum 6 years of relevant operational clinical trial experience required
- A scientific or technical degree preferred
Benefits
- Health insurance
- 401(k) matching
- Paid time off
- Professional development