LPN- Adverse Drug Events- Remote
Core
Review, document, and submit adverse drug event reports to pharmaceutical manufacturers and the FDA to ensure patient safety and regulatory compliance.
Role type
LPN Adverse Drug Event Specialist
Builds
Regulatory compliance reports and documentation for pharmaceutical manufacturers and the FDA
Domain
Healthcare / Pharmaceutical Regulatory
Required skills
Medical terminology, clinical protocols, regulatory standards, Microsoft Office, written communication, attention to detail
Preferred skills
Pharmacy or healthcare operations experience, professional certifications, independent work capability
Responsibilities
Review and assess adverse event cases, complete timely reporting to manufacturers and FDA, respond to information requests, track reporting activities and identify errors, participate in audits and quality initiatives
Seniority
Entry-level (0-2 years experience)
