An international medical devices company is looking for a Patient Safety Specialist. The qualified candidate will oversee the receipt, processing, and quality review of expedited safety reports. This position is based in Osaka.
Track adverse events
Establish and manage project files
Engage with regulatory authorities and project teams
Enter safety data into databases
Review adverse events for accuracy
Write patient narratives
Understand safety database conventions
Participate in signal detection and recognition of trends and patterns
Prepare pharmacovigilance reports
Bachelor’s degree or above (life science is ideal)
More than 2 years of PV experience
Possess valid authorisation to work in Japan
Proficient in Japanese
About the Company:
A company specialising in a wide range of services and solutions in the healthcare and diagnostics industry. They provide innovative technologies, diagnostic testing, and data-driven insights to support medical professionals and improve patient outcomes.
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