Clinical Start up Specialist – Rotterdam

Company Description

Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a Start up Specialist in Rotterdam.

Job Overview

• Responsible for CA & Ethics Committee (EC) submission
• Keep up to date knowledge of GCP and ICH Guidelines for clinical research.
• Translation and co-ordination of translations for documents required for submissions.
• Supervising study conduct according to GCP requirements and all applicable laws.

Tagged as: start up jobs