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Sona***********
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Spain
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Last Update: 11.06.2019 at 10:43
Job Type
Full Time
Start
May , 2019
Duration
6 Month
Place
Barcelona, ES
Country
Spain
Category
Description
Your Responsibilities Include, But Not Limited To Lead assigned cross functional and CMO&PS projects. Act as process owner for assigned higher complexity pharmacovigilance processes Author and maintain procedural documents for assigned processes and drive continuous improvement by alignment of relevant stakeholders globally and locally Develop and maintain training material and communications for Novartis group and third party associates. Support impact assessments on emerging regulations and ensure ongoing compliance to global regulatory requirements Lead assigned process improvement initiatives including IT projects/systems (leading enhancements and managing releases). Analyze the impact of other process and organizational changes. What You’ll Bring To The Role Minimum requirements Bachelor's or Master's degree in Pharma, life sciences or equivalent. Fluency in English. Knowledge of other languages desirable. Excellent knowledge of clinical trials regulations and processes. Minimum 4 - 7 years of experience in the pharmaceutical industry, particularly pharmacovigilance. Experience in project management and demonstrated ability to lead work groups in a matrix environment. Ability to deal and interact with a wide variety of people at all levels. Strong organizational skills togethwer with strong negotiation, presentation and communication skills,