Pharmacovigilance Auditor – Freelance (1FTE, 0.6 FTE and above)

Job not on LinkedIn

🔥 1 hour ago

🇷🇸 Serbia – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🔎 Auditor

👻 Ghost score 16%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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ERGOMED

WebsiteLinkedInAll Job Openings

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, including 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 • Conduct both remote audits and audits requiring travel across Europe

🎯 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 • Travel will be required for audits • Freelance basis; availability for 1 FTE or 0.6 FTE and above

🏖️ Benefits

• Professional growth encouraged • Supportive, collaborative work environment • Opportunity to make a real impact across the industry • Collaboration with respected pharmaceutical and biotechnology companies • Diverse and inclusive workplace where every voice counts • Work alongside experts in clinical research, pharmacovigilance, and quality consulting