Pharmacology Associate

Job Description

Responsibilities include:

• 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 and 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 that cannot do so on their own.

Requirements:

• BA degree required with 1-3 years of Safety/Pharmacovigilance Data experience.
• Argus experience is required.
• Proficiency in Outlook and Excel is also necessary.

Additional Information:

This is a one-year assignment with no travel required. The most critical skills needed are data entry and Argus experience.

We are an equal opportunities employer and welcome applications from all qualified candidates.