Sundhedsfaglig akademiker til vurdering af lægemiddelsikkerheden på europæisk niveau

This mid-level position requires a health sciences academic professional specializing in the assessment of medication safety at the European level. The role demands expertise in evaluating pharmaceutical safety data, understanding regulatory frameworks governing medicines within Europe, and applying scientific and clinical knowledge to ensure drug safety and efficacy. Candidates should possess strong analytical skills to interpret complex health data and contribute to risk assessment processes. Familiarity with European Medicines Agency (EMA) guidelines, pharmacovigilance practices, and relevant health legislation is essential. The role likely involves collaboration with multidisciplinary teams across European health authorities, requiring excellent communication skills and the ability to present findings clearly to both scientific and regulatory stakeholders. A background in health sciences, pharmacy, medicine, or related fields with experience in drug safety evaluation is implied. The candidate should demonstrate proficiency in reviewing clinical and post-marketing safety data, identifying potential risks, and supporting decision-making processes to enhance public health protection. Overall, this position suits a health professional with a solid foundation in medication safety assessment, regulatory knowledge, and experience working within or alongside European health regulatory environments.