Pharmacovigilance Auditor – Freelance Position

Job not on LinkedIn

🔥 57 minutes ago

🇪🇸 Spain – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🔎 Auditor

👻 Ghost score 20%

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Logo of ERGOMED

ERGOMED

1001 - 5000 employees

Founded 1997

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

ERGOMED is a global group providing specialized services to the biotechnology and pharmaceutical industries. It operates under different service lines, including Ergomed Clinical Research, PrimeVigilance, and ADAMAS Consulting, and is dedicated to providing full-service clinical research organization (CRO) capabilities. Focused on oncology, rare diseases, and complex trials, it also offers end-to-end pharmacovigilance and medical information services, as well as comprehensive GxP audits. Ergomed is committed to supporting drug development with a global presence in around 100 countries.

📋 Description

• Plan, prepare, conduct, report, and follow up on various types of Pharmacovigilance audits • Develop and follow up on CAPA plans • Execute audits based on comprehensive understanding of regulatory requirements and Good Pharmacovigilance Practice (GVP) • Perform GVP quality assurance projects for pharmaceutical and biotechnology client companies

🎯 Requirements

• Experience in conducting and leading internal and external Pharmacovigilance audits for a variety of stakeholders • Expert knowledge of national and international Pharmacovigilance legislation and guidelines • Proficient in managing projects and ensuring deliverables are provided timeously • Ability to identify issues and offer solutions in a pragmatic way • Bachelor’s Degree in Life Sciences preferred • Up to 40% travel • Ability to conduct remote audits

🏖️ Benefits

• Freelance position with full-time (1 FTE) or part-time (0.6+ FTE) options • Remote work in Spain • Ability to conduct remote audits • Up to 40% travel • Supportive, collaborative environment • Professional growth encouraged • Opportunity to make an impact across the pharmaceutical and biotechnology industry • Collaborative team of experts in clinical research, pharmacovigilance, and quality consulting

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