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






QUALIFICATIONS:

  • BA degree required with 1-3 years of Safety/Pharamacovigilance
  • Data experience.
  • Argus experience.

Feel free to forward my email to your friends/colleagues who might be


available.


Please Contact Me @ 732-429-1635






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