Offer summary
Qualifications:
Bachelor's degree in medicine or related field, Over 3 years of PV experience, Experience in the pharmaceutical industry or CRO, Comprehensive knowledge of drug development regulations, Native Japanese and business English proficiency.Key responsabilities:
- Lead project initiation and documentation preparation
- Manage timelines and review outputs
- Oversee team members' task statuses
- Create and review safety periodic reports
- Conduct literature screening reviews