Your overall focus is to deliver high quality case handling for internal stakeholders and authorities in order to comply with local legislation and conventions. More specifically, you will process adverse events reported worldwide on Ferring’s marketed products and development products in clinical trials. Your primary tasks will include:
We are looking for a profile that already has experience within the pharmacovigilance case handling area. You have a relevant educational background e.g. Master in pharmaceuticals /science, nurse or similar and are fluent in English both written and oral. As you play a key role in upholding our license to operate, you must have a genuine quality mindset backed by the overview and attention to detail, to ensure high quality data entry.
Additionally, it would be considered an advantage if you also have: