Global Pharmaceutical Company with main headquarters based in Japan.
Safety evaluation of collected adverse drug reaction cases
Examination and planning of safety assurance (revision of package insert, etc.) based on safety evaluation of accumulated adverse drug reaction cases
Periodic safety reports and preparation of RMP (Pharmaceutical Risk Management Plan)
Interaction and negotiation with authorities (PMDA etc) regarding safety measures and negotiate from a medical point of view.
【WHY YOU SHOULD APPLY】
Opportunity to work overseas (US and Europe)
Diverse working environment
Work with a Global Team
Flexible working hours (Flextime System)
Excellent Salary package
Medical License ( Japanese or Foreign license is acceptable)
At least 4 years Clinical Experience
Business level (N2) and above Japanese language skills
Excellent communicator with strong negotiation skills