Drug Safety Specialist III

Worldwide Salaried Open

Responsibilities:

Perform case processing activities (triage, data entry, report distribution) as required.
ssess, process, and data enter all AE case types to meet compliance requirements.
Perform triage on all case types to determine prioritization (if requested by Purdue).
Identify adverse events, seriousness, and listedness / labeledness for case assessment; review additional incoming information to determine reportability.
Select the appropriate as reported causality and company causality.
Perform all appropriate coding using MedDRA, WHO-DRUG, and Company Product dictionaries.
Own case narrative - create narrative text as required for medical orientation.
Determine follow-up requirements and request follow-up as appropriate (e-mail, phone call, letter, etc.) to request additional information.
Perform CRO case QC activities, reconciliation etc. as required.
Work on highest priority or assigned cases using Workflow Management System, or as directed.
Support PV inspections and audits as identified, including interviews and provision of requested data.
Monitor vendor KPIs/KQIs as designated by Purdue and in compliance with company guidelines and policies.
Perform additional tasks as assigned. Work independently, assess matters, propose resolutions, and appropriately escalate internally within Purdue organization.

Requirements:

Bachelor's degree (advanced degree preferred) in life science or healthcare (e.g., nursing, pharmacy).
Minimum 5 years of experience in a pharmaceutical/biopharmaceutical company.
Minimum 3 years in Drug Safety Operations role.
Experience overseeing CRO teams of case processors preferred.
US FDA pharmacovigilance inspection experience preferred.

Necessary Knowledge, Skills, and Abilities:

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