Archiviertes Projekt -  PV / Pharmacovigilance Safety Lead

General Data:
Laufzeit: 6 Monate ( voraussichtlich bis Ende des Jahres)
Auslastung: 32-40 h/ Woche
Einsatzort: 100% remote
Starttermin: ASAP

Main tasks

Support the head of department in day-to-day work as Safety Sciences Lead
Preparation and organization of workshops for employes in the area (Aggregate Reporting, PV Writing, Products and process)
Process integration support : SOP reviews, literature review
Be the voice as a contractor in discussions and for professional questions
GRIP ( Global Research in Paediatrics) Impact assessments
Support Implementation of Reg Changes ( support and organize the GPRO team)
Support MedRA Coding Integration
Support ICSR Review
Secretary of Cross-Functional Forum


Qualification

Broad experience in PV
Leadership mindset
Experience in literature review
Experience in QPPV Office (not mandatory)
Very good English skills (as primary means of communication)
precise and organizational way of working