i-Pharm Consulting

EU QPPV

Location
England
Salary
Negotiable
Posted
05 Dec 2018
Closes
19 Dec 2018
Ref
NS4829
Contract Type
Permanent
EU QPPV
Based ideally in Italy, Poland, Bulgaria, Spain, Croatia

Can be Home based
Company- CRO
3 year FTC

Salary: £Negotiable with discretionary bonus


INTRO:

A fantastic opportunity has arisen for an experienced EU QPPV to a join a top global CRO. The right candidate will be based within a non-UK EU Member State due to the UK’s future plan to withdraw from the EU.

The suitable candidate will have strong experience in a senior pharmacovigilance role and have strong understanding of EU regulations within PV. This is truly a growing company that offers a chance to work in a variety of clinical trials from Phase I to post-marketing in a variety of therapy areas.



Responsibilities include:

* Working with selected clients in accordance of the EU Directive 2001/83/EC and EU regulatory guidance
* Contributing to aggregate report writing, signal detection and literature surveillance
* Supporting PV activities at a nationally
* Process improvement and delivery of training
* Involvement in the development of client proposals and carrying out presentations at business development meetings for potential clients
* Budget oversight and working for both new and existing EU QPPV service clients



Requirements:

* Life Science degree
* Previous EU QPPV experience
* Strong knowledge of EU regulations
* Proven experience to establish processes and procedures and oversee effective PV Systems
* Experience with inspections and audits
* Must have experience to manage stakeholders
* Strong project management experience
* Experience with scientific writing
* Strong English communication skills
* Must have good client facing skills

To Apply
If you would like to discuss this vacancy further, please call i-Pharm Recruitment Consultant Niki Sansoy on +44 (0)20 3189 0470 or email nsansoy@i-pharmconsulting.com.

ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.

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