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Pharmacoviligance (PV) Consultant - Netherlands  

Company managed [?] Still accepting applications

Posted on : 22 December 2017

Project Description

Job description
We offer a job as a Pharmacovigilance (PV) Consultant, in which you will:
- work in an international environment of pharmaceutical and medical device industry
- write and review pharmacovigilance-related documents (eg. PSUR, RMP, SOPs, PSMF)
- ensure compliance with safety-related marketing authorisation commitments and obligations
- monitor and interpret safety findings from literature
- manage and maintain pharmacovigilance databases
- provide input on safety for clinical development
- be mentored by Zwiers
- live up to the Zwiers “professional approach with a personal touch” spirit

Profile
You have:
- preferably, a PhD in Pharmacy, Medical Biology, Life Sciences
- minimal 2-3 years of experience in the pharmaceutical industry and PV
- knowledge of pharmacovigilance, pharmacovigilance systems and GVP modules
- eager to learn, develop and excel
- the ability to handle deadlines and changing priorities in a dynamic environment
- writing and reviewing skills (English)
- the ability to communicate effectively based on scientific knowlegde

Offer
Zwiers Regulatory Consultancy offers a fulltime job, but is willing to discuss a part time contract
Salary will depend on education, knowledge and experience

Contact
For further information you can contact Alex Zwiers, CEO, at tel. +31 (0) 610489150.
We look forward to your application. You can apply via email: info@az-regulatory.com.