Responsibilities:
* Completing case processing, including triaging, data entry, coding of AEs, narrative writing, quality control and submission of expediting AE reports to health authorities;
* Performing case prioritization according to relevant Standard Operating Procedures to ensure timely submission of expediting reports to regulatory authorities;
* Identifying missing information and initiating follow up requests in collaboration with Drug Safety Physicians;
* Performing and overseeing reconciliation activities.
Qualifications and Experience:
* Relevant Swiss working / residency permit and / or Swiss / EU-Citizenship required;
* University degree in life sciences (pharmacy, nurse) or equivalent education in health-related field;
* At least 5 years' experience in safety or clinical data management;
* Knowledge of medical terminology and general understanding of disease processes;
* Solid knowledge of coding thesauri and medical / drug dictionaries;
* Good knowledge of the EU and US safety reporting requirements;
* Fluency in English, both verbal and written.
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