Our multinational partner is looking for a
with fluent English knowledge in their Shared Services Centre in Budapest.
- Triage of Safety Information
- Global review of non-serious cases
- Quality Control on ICSR Management
- To perform processing of adverse event safety reports in English from Source documents to the ARISg safety database.
- Perform MedDRA Coding and product coding
- Write a comprehensive case summary/safety narrative
- Management of Safety mailbox
- Fluent English
- University Degree in Life Sciences/Health care
- Minimum 5 years' relevant experience preferably in clinical function (hospitals, pharmacy) or clinical research area (CRA, Pharmacovigilance, Clinical data management, Medical writing)
- Experience in people and project management is a must!
If you are interested in the prosition, please send your application in English to the e-mail address below.