The Role
The Associate Director will manage multiple studies and projects and will be a core member of the clinical operations team.
1. Lead the clinical trial strategy, operations, and large-sized global project teams with innovative and strategic perspective.
2. Demonstrate strong stakeholder relationship, a positive working culture and act as a senior mentor within the team and company.
3. Show accountability for successful project execution and delivery of the clinical operation plan adhering to budgets, timelines and standards.
4. Ensure all trial management activities are completed in accordance with SOPs and ICH-GCP.
You
5. Extensive experience in Clinical Research within a Pharmaceutical/Biotechnology or CRO industry environment, as well as a significant time of in-depth clinical trial management and team management included.
6. Substantial project management experience.
7. Previous proven experience of all aspects of clinical study preparation and startup (including budget planning).
8. Must have experience in executing the complete range of clinical trial activities from startup to final study report.
9. Experience in oncology or immunology is preferred but multiple therapeutic area experience would be considered.