Regional Patient Safety Head Europe - Uxp-860

Detalles de la oferta

Summary:About the Role:The Role: Are you ready to step up and become the Regional Patient Safety Head of Europe? This is a senior executive role that involves strategic leadership, regulatory compliance, and operational excellence. You will ensure the safety of products throughout their lifecycle. The successful applicant will be a dynamic leader who can drive innovation, foster a culture of safety, and represent the company at the highest levels both internally and externally. As a star performer, you look to reduce case processing times and increase efficiency through process simplification, automation, and harmonization. New technology will enable innovative practices in pharmacovigilance, and you will develop top talent within the business.Key Requirements:Strategic Leadership: Co-design and lead global and local pharmacovigilance strategies across the European organization.Lead the development of safety policies and procedures to ensure regulatory compliance.Operational Management: Be responsible for the collection, evaluation, and reporting of adverse event data from clinical trials and post-marketing sources.Ensure robust safety signal detection, risk assessment, and management processes.Regulatory Compliance: Ensure compliance with global, regional, and local pharmacovigilance regulations and guidelines.Maintain up-to-date knowledge of evolving regulatory requirements and industry best practices.Talent and Team Development: Lead, mentor, and develop a successful pharmacovigilance team.Promote a culture of continuous learning and professional development.Innovation and Technology: Drive the adoption of advanced technologies and automation to enhance pharmacovigilance operations.Identify and implement innovative approaches to safety data collection and analysis.Your Experience:Advanced degree in life sciences, medicine, or pharmacy with 10+ years of experience in pharmacovigilance, drug safety, or a related field within the pharmaceutical or biotechnology industry.Experience with global pharmacovigilance regulations and compliance.Proven track record in leading and handling large, diverse teams.Significant experience in strategic leadership roles within multinational pharma companies.Expertise in pharmacovigilance processes, risk management, and regulatory requirements.Ability to cultivate successful teams and lead through change.Ability to lead and influence partners, as well as represent the organization internally and externally.Ability to drive innovation and implement advanced technologies.Proficient in English.Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.Join our Novartis Network:Division: DevelopmentBusiness Unit: PharmaceuticalsLocation: SpainSite: Barcelona Gran VíaCompany / Legal Entity: ES06 (FCRS = ES006) Novartis Farmacéutica, S.A.Alternative Location 1: GermanyFunctional Area: Research & DevelopmentJob Type: Full timeEmployment Type: RegularShift Work: NoNovartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
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Fuente: Whatjobs_Ppc

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