Clinical research assistant (cra) m/v

We are looking for a clinical safety associate h/f to work 6 months on a project for a pharmaceutical company in the area of wavre.

general description:
data-entry activities of clinical trial serious adverse events cases and some quality control related activities:
- reconciliation between clinical and safety databases.
- other administrative tasks for the case management group.

required education & skills:
•scientific degree or equivalent through experience.
•inexperienced graduates who want to put their first steps in the clinical research domain are certainly welcome as well.
•good knowledge of pharmacovigilance (basic principles, processes, systems and guidance) would be an asset - or ability to learn.
•good knowledge of english (written and spoken).
•excellent organization, administrative and database (excel) skills.
•flexible personality, proactive attitude and highly motivated.

Clinical research assistant (cra) m/v werd geplaatst in de rubriek Onderwijs te koop.
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