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Pharmacovigilance expert
Habilidades

Senior Safety Science Specialist
Fortrea Drug Development • Período integral
Feb 2022 - Mar 2026 • 4 yrs 1 mo
Assist in or complete per the Safety Management Plan (SMP) the processing of all adverse event reports from any source. ➢ Assist in producing queries of safety data for clients as appropriate. ➢ Assist Data Management or clients on reconciliation of safety databases. ➢ Possess knowledge of other procedural documents, e.g., SOPs, and how they impact safety. ➢ Demonstrate role-specific Core Competencies on a consistent basis. ➢ Assist in the preparation of client meetings and liaise with clients where appropriate