Pharmacovigilence Associate - South East UK - to £25K

An exciting pharmaceuticals company in Cambridge is looking to hire a Pharmacovigilance Associate to join their team on a permanent basis.
The company is currently involved in some interesting research into alternative therapies for unmet medical needs and as such requires and enthusiastic and dedicated individual to join their team.
You will be working on a global level ensuring the safety of these therapies in both clinical trials and post-marketing settings.
Following an impressive training programme, you will be responsible for the following:
· Data entry, review and assessment of adverse events reports using the global safety database
· Literature review for current products
· Authoring of standard operating procedures and contributing to the Pharmacovigilance processes
· Creation of safety reports for regulatory dossiers ensuring quality control at all times.
In order to be considered for this role you must be able to demonstrate the following:
· Life-science degree with a strong understanding of medical terminology
· Excellent attention to detail, be well-organised and able to deal with conflicting priorities
· Keen to broaden your knowledge in drug safety

Due to the nature of the role, you will also be required to demonstrate excellent communication skills both oral and written including narrative writing.

This is a fantastic opportunity for someone looking to make their first move into Pharmacovigilence following previous experience in pharmaceuticals. Alternatively, exceptional recent graduates will also be considered.

For a confidential discussion about this role contact Emma on 01279 657716 or emma@seltekconsultant.co.uk

Job Ref: 8738



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