Lead Start up Specialist Belgium – office based

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 Lead Start up Specialist in Belgium.

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.

Key Requirements

• Bachelor degree in life-science
• Min 1 year in EC & CA submissions within a CRO, Pharma, Biotech in Belgium
• Experience in clinical studies phase II-III
• Fluent English, Dutch & French
• Excellent communication skills
• FTE: 1.0