Administrativ medarbejder søges til arbejdet med ansøgninger til markedsføringstilladelser for lægemidler

The position requires a mid-level administrative professional experienced in managing applications for marketing authorizations of pharmaceuticals. Key competencies include strong organizational and administrative skills to handle complex documentation and regulatory submissions accurately and efficiently. The role demands familiarity with regulatory frameworks governing pharmaceutical marketing approvals, ensuring compliance with relevant laws and guidelines. Attention to detail and the ability to coordinate with multiple stakeholders, such as regulatory authorities and internal teams, are essential. Proficiency in preparing, reviewing, and submitting application dossiers and related correspondence is critical. The candidate should be adept at managing timelines and tracking application statuses to meet deadlines. Strong communication skills, both written and verbal, are important for liaising with external agencies and internal departments. While specific educational requirements are not detailed, a background in life sciences, pharmacy, or a related field combined with administrative experience in the pharmaceutical or healthcare sector would be beneficial. Experience with regulatory databases, document management systems, and standard office software is expected. Overall, the role suits a detail-oriented, organized individual capable of navigating regulatory processes and supporting the marketing authorization workflow for medicinal products.