Our client is looking for Drug Safety Data Management Specialist – with the Argus experience!
RESPONSIBILITIES:
• 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 Drop in Data Entry II application.