Xendo Xendo DeutschlandXendo Deutschland

Contact info

Human Resources Department
T: +31 (0)71 524 40 00
E: hr@xendo.com



As Vigilex is steadily growing we are looking for new colleagues to strengthen our global and local teams.

Consultant Pharmacovigilance 

In this role you will support us in providing our clients with services in the area of:

Adverse Event Management, Risk Management, Signal Management, Periodics, Qualified Person responsible for Pharmacovigilance (QPPV) services, Audits and Training services. Currently there are different vacancies available. We work with a wide variety of pharmaceutical companies worldwide.
You have a broad experience within  pharmacovigilance, preferably in an EU or global setting and with different companies or a regulatory authority. Experience in auditing or other fields in the pharmaceutical industry such as clinical development/operations or regulatory affairs is a plus.
You have a medical or paramedical background or a degree in life sciences in combination with a solid knowledge of European pharmacovigilance regulations. You are able to work independently and  within strict timelines, and you are able to manage your own priorities within the assigned client projects. You are an excellent communicator,  you have attention to detail and  good analytical skills. You enjoy working in a variety of fields and are able to adapt to different company settings and client needs.
As our clients are based globally, you should be willing and able to travel abroad on a regular basis.  You are fluent in English (verbal and written). The role is not location bound. You reside in the EEA. You can work home-based and will have the opportunity to visit our office in The Netherlands at least twice a year for training and team meetings. You will be part of a network of senior PV staff that will support you wherever you are.