We are seeking a PV Physician I/II (Japanese) to review and approve post-marketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports, and to work as a Qualified Person for Pharmacovigilance or support the Qualified Person in medical understanding and evaluation of safety issues.
Requirements
- Medically qualified as a physician
- Previous experience in pharmacovigilance
- Ability to review different aggregate report types
- Expertise in signal detection activities
- Excellent interpersonal skills
- Ability to plan, organise, prioritise and execute multiple tasks
- English - advanced (spoken, written)
- Japanese - advanced (spoken, written)
- Advanced literacy (MS Office)
Benefits
- Training and career development opportunities internally
- Strong emphasis on personal and professional growth
- Friendly, supportive working environment
- Opportunity to work with colleagues based all over the world, with English as the company language
