Drug Safety Data Management Specialist

• 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 company's 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 Drop in Data Entry II application on behalf of country offices cannot on their own.
• BA degree required with 1-3 years of Safety/Pharmacovigilance Data experience preferred.

BA degree required with 1-3 years of Safety/Pharmacovigilance Data experience preferred.

Sneha Shrivastava

Technical Recruiter (Clinical/Scientific)

Artech Information Systems LLC

360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960

Office: 973.967.3348 | Fax: 973.998.2599

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