Your tasks

• Review, rank, verify, process and document case-related information: event terms; validity, seriousness, special scenarios; timelines; accuracy and consistency. Process cases based on these assessments
• Review case criteria to determine the appropriate workflow for case processing
• Carry out case processing activities of adverse events/adverse drug reaction reports including writing the case narrative
• Quality control of processed cases to verify accuracy, consistency, and compliance with process requirements
• Determine and perform appropriate case follow-up, including generation of follow-up requests
• Liaise with key partners, locally, and other stakeholders regarding safety data collection and data reconciliation
• Train the employees on pharmacovigilance topics and maintain the training material

Who you are

• Bachelor of Pharmacy, Life Science or similar university degree
• Experience in a team setting or drug safety either in the pharma industry, in a health authority or at a service provider is an asset
• Excellent verbal and written communication skills, including fluency in English (German preferable)
• User skills in safety databases preferred
• Good knowledge in medical terminology
• Ability, with supervision, to solve routine problems
• Independent, reliable team player with an accurate way of working
• User skills in MS Office (Word, Excel, PowerPoint, Outlook)