About this role
Role Overview
- Supports Global Study Managers (GSMs) and other Study Operations Managers (SOMs) to deliver study management by leading specific parts of projects
- Oversees the preferred Contract Research Organization (pCRO) at country level and manages country level plans
- Liaises with Site Care Partners (SCP) and regulatory colleagues to agree on submission strategy to Health Authorities (HAs)
- Collaborates to identify and manage deviations and risks in study startup and execution
- Ensures compliance to relevant global and local, internal and external requirements, and regulations
Requirements
- Bachelor’s of Science or Bachelor’s of Arts degree with a 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
- Comprehensive knowledge in managing and coordinating specific tasks and responsibilities as part of a larger study management team
- Demonstrated clinical research experience and/or study management/startup project manager experience
- Must be fluent in English.
Benefits
- Health insurance
- Flexible working arrangements
- Professional development opportunities