Tasks

- Execution and delivery of assigned studies within Europe
- Planning, organizing and managing risks/contingency for each stage of the study
- Study oversight: coordinating internal and external operational activities, maintaining clear visibility to sites’ progress and issues, reviewing protocol deviations and metrics
- Training of in-countries staff assigned to the studies

Qualifications

- Bacherols’s Degree (or higher) in a Life Science discipline
- At least 7 years of experience clinical research, in planning/executing and monitoring of clinical trials
- A minimum of 4 years of experience in a regional/global project management role
- Experience in oncology
- Place of residence: Spain or the Netherlands
- Fluent in English