For a client of ours we are looking for a CRA (early phase)
Job description
The early phase clinical trials are executed in the Clinical Pharmacology Unit (CPU) in Antwerp. In your role, you will help coordinate the set-up and organization for these studies.
Responsibilities
- The study protocol reviews;
- The study set-up;
- Daily study aspects (such as creation, development and completion of documents, team coordination, quality control, internal and external communication and reporting, …
Profile
- You have a strong interest in medical sciences and preferably you already have some paramedical background;
- You have at least one year monitoring experience in Belgium and have a good knowledge of ICH GCP and European Directives 2001.
- You are fluent in Dutch and English, knowledge of French is a plus;
- You like situations and studies to be structured; your sense of precision and accuracy is very high;
- You like setting priorities. For every study we can count on your analyzing and synthesizing skills;
- You have excellent commercial awareness and you love to serve our customers and work together with them for the perfect result(s);
- You like leading a team, you are a good observer and an easy learner.