Pharmacovigilance / Drug Safety Manager, Cambridge career at Stelfox Recruitment in

Stelfox Recruitment is currently seeking to employ Pharmacovigilance / Drug Safety Manager, Cambridge on Thu, 12 Sep 2013 11:22:14 GMT. A role for an experienced PVG Drug Safety Manager to join a leading global CRO company in Cambridge and manage the Drug Safety Team. Duties: • You will be responsible for the planning, co-ordination, maintenance and delivery of a variety of research projects • You will maintain the compliance for aggregate and individual case safety reports • Work in collaboration with other departments to...

Pharmacovigilance / Drug Safety Manager, Cambridge

Location: England

Description: Stelfox Recruitment is currently seeking to employ Pharmacovigilance / Drug Safety Manager, Cambridge right now, this career will be placed in England. More details about this career opportunity please give attention to these descriptions. A role for an experienced PVG Drug Safety Manager to join a leading global CRO company in Cambridge and manage the Drug Safety Team.
Duties:

• You will be responsible for the planning, co-ordination, maintenance and delivery of a variety of research projects
• You will maintain the compliance for aggregate and individual case safety reports
• Work in collaboration with other departments to strive for a continuous process improvements of drug safety operations on a global level

You will need:

• A life science degree and / or nursing qualification
• Strong Pharmacovigilance/drug safety experience within the pharmaceutical industry
• A proven track record of managing a Drug Safety team

If you have the skills and experience for this opportunity and the ambition to take on this position, please call Sean for further details or email your CV today.

Contact Sean at +44 1273 727 930 or sean.ridley@stelfoxuk.com

Sean is a specialist Pharmaceutical Consultant within Pharmacovigilance. He places candidates acr! oss the UK, Europe, USA and Asia.

Key words

! Drug Safety, Pharmacovigilance, Manager, Pharmaceutical, UK, regulation, Global, SOP, SAE, PV, PVG, ICH guidelines, WPD, Associate, Officer, Audit, Case processing, Adverse events, Serious adverse events, Clinical trials, Regulatory authorities, Reporting, Development, Project, Clinical, Healthcare, Life science, reporting, cross-functional, processes, mentor, training
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If you were eligible to this career, please email us your resume, with salary requirements and a resume to Stelfox Recruitment.

If you interested on this career just click on the Apply button, you will be redirected to the official website

This career starts available on: Thu, 12 Sep 2013 11:22:14 GMT

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