Company: Docs Global (Continental Europe)
Location: WOLUWE SAINT LAMBERT,Belgium
Reference: Ref AS-019528
Closing Date: 10 Dec 16
Salary (£): Competitive
Benefits: Excellent & Comprehensive
For an immediate consideration please send your most recent resume to email@example.com This is an excellent opportunity that should not be missed, don’t miss out and apply today!
Roles & Responsibilities of the position
The Pharmacovigilance activities include but not limited to: the processing of individual serious adverse event reports, preparation of annual safety reports, implementation and maintenance of the Pharmacovigilance procedures and safety database, transfer of Pharmacovigilance data, support to others units, education and trainings.
Other responsibilities :
Participates in the Eudravigilance Expert Working group.
Represents our client at the MedDRA Usergroup meetings
A scientific university degree in Medicine, Pharmacy, Bioscience or equivalent
3-5 years in Pharmacovigilance and risk management
Good organization and negotiation skills
Deep sense for responsibility and high degree of self-motivation
Good communication skills with the ability to communicate with diverse individuals and groups. Fluent English (spoken and written)
Knowledge of European PV reporting regulations
Demonstrates computer literacy with proficiency in the used and management of safety databases
Permanent contract with our client.
Base salary with extra benefits as medical insurance, pension, meal vouchers and extra vacations days
2 Globeside, Globeside Business Park
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