Patient Safety Specialist I (Pharmacovigilance) – Contract
Plainsboro, NJ (Onsite – Mon–Fri, with occasional flexibility)
$28.00/hr on W2 | 6-Month Assignment
We are seeking a detail-oriented Patient Safety Specialist with strong pharmacovigilance experience to support adverse event case processing and ensure compliance with safety reporting standards.
Key Responsibilities:
- Process and manage adverse events (AE) and technical complaints
- Perform MedDRA coding, case triage, and narrative writing
- Handle inbound/outbound calls with patients, HCPs, and stakeholders
- Maintain accurate data in drug safety databases (e.g., Argus)
- Support case quality review, follow-ups, and compliance with FDA reporting
Must-Have Requirements:
- Bachelor’s in Life Sciences / Medical field or RN with clinical experience
- 2+ years Pharmacovigilance experience (AE processing + MedDRA coding)
- Strong knowledge of medical & drug safety terminology
Nice to Have:
- Experience with safety databases / call center environment
- Exposure to audits/inspections
- Background in diabetes, obesity, or related therapeutic areas
