Regulatory Consultant - PV

You:

• have a PhD in Pharmacy, Medical Biology, Life Sciences
• have 5 years of experience in PV
• will ensure compliance with safety-related marketing authorisation commitments and obligations
• will take on the role of QPPV will write and review pharmacovigilance-related documents
• will review safety findings from literature and manage pharmacovigilance databases

We:

• stimulate you to give us a call before applying
• offer a working environment in which a professional approach goes hand-in hand with a personal touch
• invite you to apply by This email address is being protected from spambots. You need JavaScript enabled to view it. your CV and motivation.

Check out the detailed description!