European QPPV - Paris - Office Based
Our Client is a specialist consultancy that works with start-ups to mid-size companies to bring products to the market in the most efficient and cost-effective manner.
The company assists pharmaceutical, medical technology and biotechnology companies in the design and implementation global regulatory strategies to ensure compliance and a smooth entrance to market and beyond
You will have oversight of the PV systems in terms of structure and performance, case processing and medical review including QC and QA procedures.
The EU QPPV will perform the following activities on behalf of the Marketing Authorization Holder.
Responsibilities will include:
You will need to have experience in Pharmacovigilance at a senior level and also have experience in a QPPV role.
Keywords: Qualified Person, Pharmacovigilance, France, Drug Safety, European QPPV, Office Based, QPPV, EU, EEA, Medical Doctor, Physician, Médecin Pharmacovigilance, Medicine, MD, Industrie du médicament humain, Ile-de-France, Paris
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