Job Description

Supervise PV team including the coordination of the Local Qualified Person Responsible for Pharmacovigilance (QPPVs). Review the PV components of all domestic study protocols. Review all local patient support programs and other undertakings of the local organization with potential consequences on PV . Represent PV system on a local level and for the countries in his/her jurisdiction. Assure the collection, review, processing and distribution of adverse event information. Defining and ensuring execution of the Pharmacovigilance strategies for sedico products where applicable. Assuring a robust and healthy local Pharmacovigilance system with regulatory compliance and proactive audit and inspection readiness and on time/comprehensive management of observations..

Requirements:

8 - 12 years of experience, in the pharmaceutical industry. Bachelor of Pharmacy or Science "Strong attention to detail. Good mathematical skills. Teamwork Problem Solving. Good Communicator. Commitment to Safety V. Good English. Good Computer / other softwares sills"