PV Operations Specialist
SystImmune · Princeton, NJ · 6 days ago
On-siteManagement$85k–$115k/yrFull-time
Key Responsibilities
- Perform intake, triage, data entry, and quality review of ICSRs.
- Ensure timely regulatory submissions in accordance with global requirements.
- Maintain accuracy and completeness of safety data in the PV database.
- Collaborate with cross-functional teams to support audits, inspections, and CAPA implementation.
- Follow SOPs, work instructions, and applicable regulations (e.g., FDA, EMA, ICH).
- Support continuous improvement initiatives within PV operations.
- Facilitate the generation of listings for the periodic safety reports (e.g., DSUR, PSUR).
- Work with the QA department to maintain a state of high PV inspection readiness across all regions/countries.
- Support the performance of root cause analysis of deviations relevant to PV systems.
- Prepare responses to audit findings that concern the PV department.
- Manage reconciliation activities with other departments within the company and vendors.
Qualifications
- Bachelor’s degree in life sciences, pharmacy, nursing, or related field.
- 3-5+ years of experience in pharmacovigilance case processing preferred.
- Familiarity with safety databases (e.g., ArisG, Argus) and regulatory reporting requirements.
- Strong attention to detail, organizational skills, and ability to work independently.