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Pharmacoviligance (PV) Consultant Oss Netherlands,  

Pivot Park (company)


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.

Locations

5349 AB Oss, Netherlands

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