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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.
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.
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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