Description
- Enter applicable information into the global safety database for initial or follow up cases received via paper, fax or email.
- Book-in, quality check, and initially assess cases from suppliers sending cases via paper, email or fax.
- Accept cases from European Health Authorities on behalf of Country Offices that are not online, and other submitters as necessary.
- Monitor electronic mailboxes to ensure timely acceptance of reports.
- Perform data entry into databases, as needed.
- Ensure proper coding of events and drugs for cases to ensure correct forwarding to the relevant Therapeutic Area Teams and Licensing Group.
- Upload reports on behalf of country offices that cannot on their own.
SKILLS:
- BA degree required with 1-3 years of Safety/Pharmacovigilance Data experience.
- Attendance within this position is critical.
- MS Excel, MS Outlook, MS Word.