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