Pharmacovigilance Technician (Remote in Cary, NC)

Pharmacovigilance / Adverse Event Reporting Specialist (Pharmacy) — Cary, NC (Hybrid onboarding → Remote)

Location: Cary, NC (must be within 60 miles)
Work setup: Remote after training (1 week onsite onboarding in Cary + 1 week onsite 1:1 training with Lead, then remote)
Schedule: 40 hrs/week — 9:00am–6:00pm ET or 10:00am–7:00pm ET
Pay rate: $25.00/hr

Overview

We’re hiring for a detail-oriented pharmacy/clinical professional to create and submit Adverse Event (AE) and Product Complaint (PC) reports using information documented in a patient management system. This role focuses heavily on quality review (QC), accuracy, and reconciliation reporting to biopharma stakeholders.

What you’ll do

• Create and submit AE and PC reports from patient management system documentation
• Perform daily quality checks (accuracy, spelling/grammar, drug/manufacturer details, completeness)
• Communicate with clinicians to resolve questions or improve documentation quality
• Identify missing AEs/PCs and ensure they’re properly submitted and tracked
• Prepare and submit weekly/monthly reconciliation reports per client requirements
• Support clinical auditing efforts by helping identify trends/issues in reporting
• Perform other duties as assigned

Required skills

• Strong written and verbal communication
• Excellent organization, time management, and attention to detail
• Comfortable with moderate to advanced computer skills
• Strong Excel/spreadsheet skills
• Ability to multitask and work effectively with others
• Flexible/adaptable
• Ability to type quickly and accurately (numeric + text data entry)

Preferred qualifications

• Pharmacy setting experience (preferred)
• Pharmacovigilance experience (AE/PQC reporting) (strongly preferred)
• Pharmacy Technician or other clinical background (preferred)
• Oncology experience (plus)
• Bachelor’s degree or equivalent experience (preferred)

How to apply

Reply with your resume and a brief note on your experience with AE/PQC reporting and/or pharmacovigilance.