Regulatory Affairs Specialist

Responsible for the creation, preparation and submission to the regulatory agency: Prescribing Information and Promotional Materials. Ensure that the information contained in the promotional materials complies with local regulation: printed/digital materials, digital campaigns, web pages. Support with regulatory processes regarding product maintenance.
About the RoleMajor Accountabilities:
To ensure the smooth running of the Drug Regulatory Affairs Department through providing professional secretarial service and assistance, and to contribute to the achievement of functional objectives.Learns to use basic principles, theories, and professional concepts.Contacts are primarily with immediate supervisor and other personnel in department or group.Works on problems of routine scope. Follows established policies and procedures.Normally receives detailed instructions on all work.Key Performance IndicatorsAdherence to Novartis policy and guidelines.Project & stakeholder feedback.Work Experience- Gestión y ejecución de Operaciones
- Gestión de proyectos
- Amplitud funcional
- Experiencia multicultural
Skills- Bases
- Planificación de proyectos
- Colaboración
- Ciencias biológicas
- Orientado a los detalles
- Cumplimiento normativo
LanguageInglés
Why Novartis:Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients' lives. Ready to create a brighter future together? Learn more.
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Functional Area: Research & Development
Job Type: Full time
Employment Type: Regular
Shift Work: No

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