Knowledge of safety guidelines and regulations for medical devices and/or pharmaceutical development and post-market surveillanceFamiliarity with medical terminology and working with large databases.Proven ability to analyze, interpret, and discuss safety information relating to multiple therapeutic areas.Strong interpersonal, effective communication (written and verbal), and presentation skills.Strong organization and time management skillsDemonstrates attention to detail and accuracy.Self-motivated, ability to work under pressure, demonstrating initiative and flexibility.High learning agility, ability to work independently and meet targeted timelines in a team-centric environment.Experience with (safety or others) issue management

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