Description
We are seeking a Pharmacovigilance Intern to assist with drug safety data processing and project workflow management.
Responsibilities:
- Assist in handling adverse event safety data, including collecting and tracking incoming adverse event information, determining initial or updated event status, and monitoring event processing timelines.
- Support project workflow management, including database entry, quality control activities, and generating pharmacovigilance reports.
- Perform other tasks assigned by supervisors.
Requirements:
- Pass Japanese N2 proficiency test or equivalent level of Japanese language skills; pass university English CET4 level or above.
- Bachelor's degree or higher; Japanese majors are welcome, and those with biology or pharmaceutical backgrounds are preferred.
- Able to work at least 24-32 hours per week.
Benefits:
- Opportunity to work in a dynamic environment
- Chance to gain practical experience in pharmacovigilance
- Priority consideration for full-time offer after successful completion of internship
Location:
- Dalian office: 10th floor, West Wing, Tengfei Software Park, High-tech Zone
- Remote and on-site internship options available