Drug Safety Data Management Specialist

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 to DSS via paper, email or fax. Accept E2B cases received through the Argus Electronic Submissions Module (ESM) from European Health Authorities on behalf of Country Offices that are not online with Argus and other submitters, as necessary. Monitor electronic mailboxes and Argus ESM to ensure timely acceptance of Adverse Event (AE) 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 AE reports to the data entry application on behalf of country offices cannot on their own.

SKILLS:

Attendance within this position is critical, only a maximum of 7 days off can be accommodated. BA degree required with 1-3 years of Safety/Pharamacoviliance Data experience. MS Excel, MS Outlook, MS Word desired. Argus experience desired.