Drug Safety Data management Specialist

Drug Safety Data Management Specialist

NOTE: CANDIDATES MUST HAVE ARGUS EXPERIENCE.

RESPONSIBILITES:

• 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.
•  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 on behalf of country