Qualified Person Responsible for Pharmacovigilance, QPPV – EU, UK

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🔥 1 hour ago

🌐 United Kingdom, Serbia – Remote

🇬🇧 United Kingdom – Remote 🇷🇸 Serbia – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

👻 Ghost score 18%

What it means: the chance that no one is really hiring for this job.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

• Establish and maintain a system ensuring information about all suspected adverse reactions is collected, collated, and accessible within the Community • Ensure requests from competent authorities for additional benefit-risk evaluation information are answered fully and promptly • Provide competent authorities with other information relevant to medicinal-product benefit-risk evaluation, including planned post-authorisation safety studies • Remain continuously available to competent authorities in Member States, the Agency, and the marketing authorisation holder • Ensure adequate back-up procedures are in place • Oversee safety aspects of the company’s medicinal products • Maintain an overview of medicinal product safety profiles and emerging safety concerns • Oversee conditions, obligations, and safety commitments associated with marketing authorisations • Review relevant findings from company-conducted studies and programmes

🎯 Requirements

• Life-science education background • Medicine (human or veterinary) or Pharmacy preferred • Solid knowledge of PV system operations and function • Strong knowledge of Global Regulations, standards and best practices regarding safety processing and reporting, safety surveillance and pharmaceutical industry compliance activities in post-marketing • Strong operational and managerial skills as demonstrated by leading previous projects or functions • Strong experience in a PV role • Profound experience as QPPV • Strong oral and written English communication skills

🏖️ Benefits

• Training and career development opportunities internally • Strong emphasis on personal and professional growth • Friendly, supportive working environment • Opportunity to work with colleagues based all over the world • Equal opportunities workplace • Human-centric environment • English as the company language

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