Pharmacovigilance Executive

Paramount Recruitment Ltd

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Staffing Firms

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Address 1 :

United Kingdom,London,London,

Key Skills :

PV, drug safety, pharmacovigilance, London, slough, CRO, serious adverse events, executive, speciali

Salary :


Date Posted :

15 Apr, 2016

Company Name :

Paramount Recruitment Ltd

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Job Category :

Drug Safety Jobs

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Pharmacovigilance Executive

CRO- Slough- Drug Safety- Adverse Events- Coding- SOPs- Regulatory- Database- TMF- GCP

A fantastic opportunity has become available for an experienced drug safety professional to join the Pharmacovigilance department of a reputable CRO. The company focus on the therapeutic areas including; oncology, intensive care, organ transplant, cystic fibrosis and many more.

The company are looking for skilled and talented Pharmacovigilance professionals who are able to support the PV activities of the company and able to set up safety databases and process serious adverse events reports.

As a Pharmacovigilance Executive you will:
*Participates in client liaison
*Ensures pharmacovigilance data is processed such that subjects' rights, safety and well being are protected and that the pharmacovigilance data are reliable.
*Abide by deadlines for expedited submissions in accordance with national authority requirements
*Code serious adverse events in accordance with the medical dictionary
*Maintain the Serious Adverse Events section and PV correspondence of the TMF
*Review the quality control of the safety database
*Ensure CRAs are aware of Serious Adverse Events reported at their assigned sites
*Obtains information to clarify and support data reported in Serious Adverse Event
forms in an appropriate time frame.
*Works with Data Managers to ensure that the Serious Adverse Event data in safety databases and clinical databases are reconciled on a regular basis.

An ideal Pharmacovigilance Executive will have:

*Basic experience and knowledge of Pharmacovigilance or Drug Safety
*Graduate and Postgraduate degree in a scientific or healthcare discipline
*Understanding of clinical trials methodology
*Working knowledge of ICH GCP
*Demonstrate an understanding of the role of pharmacovigilance within the product life cycle from conception to approval
*Working knowledge of coding dictionaries used in PV
*Able to implement SOPs

This would be a fantastic opportunity for a drug safety professional to work for a global and reputable Clinical Research Organisation.

If you are interested in this opportunity and wish to discuss further details about the role or other Drug Safety and Pharmacovigilance positions in the UK and Europe, please contact Sabrina Deo at +44 (0)121 616 3471.

PV, drug safety, pharmacovigilance, London, slough, CRO, serious adverse events, executive, specialist, GCP, SOP, clinical trial, TMF, coding, dictionary, medical, case processing, GCP, scientific, healthcare, clinical, assistant, associate, officer

Paramount Recruitment Limited provides services as an agency and an employment business. We regularly have similar roles in this area. Please see our website for details or send your CV in to us to find out the latest opportunities.

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