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As an Associate Drug Safety you make sure that the rules and guidelines of our case processing are followed. Together with your Drug Safety team you ensure that all aspects of Pharmacovigilance are adhered to.

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)