Drug Associate Safety Administrator
Core
Provide contracted project coordination and safety support for global and domestic clinical programs, focusing on adverse event management, protocol inquiries, and diagnostic assessments.
Role type
Associate Safety Administrator (Clinical Operations)
Builds
Clinical trial safety documentation and reporting for pharmaceutical and biotech clients
Domain
Clinical Research / Pharmaceutical Safety
Deliverable
dashboards & analysis
Required skills
Adverse event triage, protocol inquiry management, data entry and reconciliation, regulatory compliance (FDA/ICH), meeting coordination, document redaction, LMS training management
Preferred skills
None stated
Technologies
MS Office (Word, Excel, PowerPoint, Access), electronic filing systems, learning management systems
Responsibilities
Coordinate review of protocol inquiries and triage abnormal lab alerts; manage project-specific training and system reconciliations; facilitate client meetings and maintain program files; handle incoming safety hotline calls and information routing.
Seniority
Junior, entry-level IC