Descripción de la oferta
Company Description 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. Job Summary We are currently looking to partner with a 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 requires 1 full day of auditing on a remote basis (additional hours reserved for preparation & write‑up). The audit also requires fluency in Spanish and English and ideally already working as an independent Consultant. Qualifications 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 Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto. #J-18808-Ljbffr
