With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.
Descubra exactamente qué habilidades, experiencia y cualificaciones necesitará para tener éxito en este puesto antes de enviar su solicitud a continuación.
We are currently looking to partner with Pharmacovigilance (GVP) Auditor who can partner with us to perform a critical GVP audit for one of our key clients in Quarter 2 2026 (dates are flexible within the period). This audit specifically focuses on Patient Support Programmes and it requires 1 full day auditing on a remote basis (additional hours put aside for preparation & write up). The audit also requires fluency in Spanish and English and ideally already working as an independent Consultant. xpzdshu
Extensive experience in Pharmacovigilance (GVP) auditing is required with the life-sciences sector
Demonstrated experience working on patient support programmes (from an auditor perspective) is highly preferred
Thorough experience working as a GVP Auditor is a must
Fluent in English and Spanish (verbal & written)
Can perform the audit within Q2 of 2026
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Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.