Acerca de la Empresa
Novartis is a global healthcare company based in Switzerland that provides solutions to address the evolving needs of patients worldwide. We use innovative science and digital technologies to create transformative treatments in areas of great medical need. Our mission is to reimagine medicine to improve and extend people’s lives. We are committed to fostering a diverse and inclusive environment where all associates are inspired to contribute to our purpose.
Descripción del Trabajo
Join Novartis as a Medical Writing Intern and gain invaluable hands-on experience in the pharmaceutical industry. This internship offers a unique opportunity to contribute to the creation of high-quality scientific and regulatory documents under the guidance of experienced medical writers. You will learn about drug development processes, regulatory requirements, and the art of clear, concise, and compliant scientific communication. This role is perfect for ambitious individuals passionate about science and seeking a career in medical writing.
Responsabilidades Clave
- Assist in the research and compilation of scientific data for various medical documents.
- Draft sections of clinical study reports, protocols, summaries, and other regulatory documents.
- Support the review and editing of medical texts for accuracy, clarity, and adherence to guidelines.
- Ensure compliance with internal standard operating procedures (SOPs), company guidelines, and external regulatory requirements.
- Collaborate with cross-functional teams, including clinical development, regulatory affairs, and statistics.
- Participate in team meetings and contribute to discussions on document strategy and content.
- Maintain up-to-date knowledge of industry best practices and evolving regulatory landscapes.
Habilidades Requeridas
- Currently enrolled in or recently graduated from a Bachelor's, Master's, or Ph.D. program in Life Sciences, Pharmacy, Medicine, or a related field.
- Excellent written and verbal communication skills in English.
- Strong attention to detail and ability to maintain accuracy in scientific documentation.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
- Ability to work effectively in a team-oriented environment.
- Strong organizational skills and ability to manage multiple tasks.
Cualificaciones Preferidas
- Basic understanding of drug development processes and regulatory affairs.
- Previous experience with scientific writing or editing (e.g., academic papers, theses).
- Familiarity with medical terminology.
- Knowledge of other languages relevant to the European market is a plus.
Ventajas y Beneficios
- Structured mentorship program with experienced medical writers.
- Opportunity to work on real-world pharmaceutical projects.
- Exposure to a global healthcare company environment.
- Professional development opportunities and training.
- Networking opportunities with industry professionals.
- Potential for future full-time employment within Novartis.
- Competitive monthly stipend.
Cómo aplicar
Si estás interesado en esta oportunidad, haz clic en el botón "Aplicar ahora" que aparece a continuación. Para asegurar que tu solicitud sea considerada, por favor incluye:
- Un currículum actualizado
- Una carta de presentación breve que resuma tu experiencia y motivación
Las solicitudes se revisan de forma continua. Solo los candidatos preseleccionados serán contactados para una entrevista.
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