ph3Pharmacovigilance Auditor - Freelance Position (1FTE or 0.6 FTE and above) /h3 ul liFull-time /li liDepartment: GVP Compliance /li /ul pMedicine moves forward here. So will you. /p pADAMAS Consulting helps the world's pharmaceutical and biotechnology companies uphold the highest standards of quality, compliance and patient safety. Since 2007 we have partnered with organizations across GCP, GVP, GMP, GLP and Computer Systems Compliance, and we are trusted by many of the most respected names in life sciences. /p pWe think of our work as more than auditing. At its best it is intelligence: helping clients see the compliance risks that matter most and prevent the problems that could put patients at risk. That takes sharp, independent thinking and deep expertise, which is exactly what our people bring. /p pHere your knowledge is valued and shared, not kept in silos. We have built a supportive, collaborative environment where professional growth is encouraged and where you can make a real impact across the industry, working alongside some of the most respected companies in the field. /p pADAMAS Consulting is looking for PV Auditor on a freelance basis to cover audits across Europe. Both full and tempo parziale (0.6+ FTE) will be considered /p pPlanning, preparation, conduct, reporting and follow up (including CAPA plans) of various types of Pharmacovigilance (PV) audits according to expected quality and timelines /p pExecuting audits based on a comprehensive understanding of all regulatory requirements and Good Pharmacovigilance Practice (GVP)



/p pPerforming GVP quality assurance projects on behalf of client companies within the pharmaceutical/biotechnology industry. /p pExperience in conducting and leading internal and external Pharmacovigilance audits for a variety of stakeholders /p pExpert knowledge of national and international Pharmacovigilance legislation and guidelines /p pProficient in managing projects and ensuring deliverables are provided timeously /p pAbility to identify issues and offer solutions in a pragmatic way /p pBachelor’s Degree in Life Sciences preferred /p pTravel will be required for audits, additional to conducting remote audits /p pWhen you join Ergomed Group, you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world. You’ll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting. /p pWe are diverse in many ways, yet our values unite us. Our values are how we work, not words on a wall. If they sound like you, you will feel at home here. /p pQuality: we hold ourselves to the standard patients deserve. /p pIntegrity and trust: we do the right thing, especially when it is hard. /p pDrive and passion: we care about the outcome, because someone is waiting on it. /p pAgility and responsiveness: we move quickly, because patients cannot wait. /p pBelonging: everyone is welcome, and every voice counts. /p pCollaborative partnerships: we go further by going together. /p pWe look forward to welcoming your application. /p /p #J-18808-Ljbffr

📌 Pharmacovigilance Auditor - Freelance Position (1FTE or 0.6 FTE and above) (Roma)
🏢 Ergomed Group
📍 Roma