



The Global Medical Information Specialist Intern will support the Global Medical Information function in the provision of accurate, balanced, and scientifically sound medical information. The internship offers exposure to global medical affairs activities, scientific communication processes, and cross-functional collaboration within an international pharmaceutical environment. The intern's on the job training will be supervised while contributing to core Medical Information activities and selected global projects. You’ll be involved in following activities: Medical Information Activities * Support the preparation of responses to medical and scientific inquiries from healthcare professionals and internal stakeholders, ensuring accuracy and compliance. * Conduct structured literature searches using scientific databases to identify relevant clinical and scientific evidence. * Assist in drafting, reviewing, and updating standard response documents and medical information materials. * Contribute to the maintenance of global medical information content and knowledge management systems. Scientific Documentation and Quality * Ensure documentation is complete, accurate, and aligned with internal procedures and regulatory standards. * Support quality control activities related to medical information responses and materials. * Maintain appropriate documentation in accordance with pharmacovigilance and compliance requirements. Cross-Functional Collaboration * Collaborate with Global Medical Affairs, Regulatory Affairs, Pharmacovigilance, and other relevant departments as needed. * Participate in internal meetings and training sessions to gain understanding of product portfolios and therapeutic areas. Project Support * Contribute to continuous improvement initiatives aimed at optimizing medical information processes and tools. * Support the development of training materials or internal guidance documents when applicable.