Company DescriptionFor the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world's largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. 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 DescriptionWe 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 ****** (dates are adaptable 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.Qualifications requiredMust have an education of at least BSc or higher within a life-sciences or medical disciplineExtensive experience in Pharmacovigilance (GVP) auditing is required with the life-sciences sectorDemonstrated experience working on patient support programmes (from an auditor perspective) is highly preferredThorough experience working as a GVP Auditor is a mustFluent in English and Spanish (verbal & written)Can perform the audit within Q2 of ****Excellent stakeholder management skillsAdditional informationWe celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion.