Pharmacovigilance Specialist

hace 2 semanas

Tlahuac, México IQVIA A tiempo completo

**Job Overview**Under moderate supervision, executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional, or country level.**Essential Functions**- Pharmacovigilance processes applicable to RSU.- Submission of safety reports (periodic and expedited)- Submission of SAE/SUSAR to RA on time for the applicable studies according to regulatory timelines.- Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines.- May also include maintenance activities.**Qualifications**- Bachelor's Degree Life sciences or a related field.- 1 - 2 years of pharmacovigilance experience in clinical studies.- Fluent Conversational English.

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