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vor 1 Tag

Basel, Schweiz ALBEDIS Vollzeit

EINFÜHRUNG: We offer an exceptional opportunity for a professional seeking a challenging role in a renowned, fast-growing pharmaceutical company. Our client operates at the forefront of drug safety and pharmacovigilance, delivering high-quality scientific insights to support patient-focused risk management. We are now recruiting a Senior Data Scientist - Literature to join the Safety Analytics and Reporting (SAR) team within the Safety Risk Management function. This role provides a unique opportunity to perform literature searches, contribute to safety signal detection, and support strategic initiatives in medicinal product and device safety. AUFGABENBESCHREIBUNG: • Perform ad-hoc and systematic literature searches in biomedical databases to identify adverse drug reactions and safety risks • Develop, test, document, and maintain search profiles for regulatory reporting, including DSURs, PBRERs, and MDIRs • Conduct efficacy searches for Pharma Development Medical Affairs (PDMA) and support cross-functional teams with timely, accurate results • Create training materials for team members and stakeholders on literature retrieval and reporting best practices • Actively contribute to process improvement, knowledge sharing, and cross-functional collaboration within the Safety Literature Group ERFORDERLICHES PROFIL: • M. S. or University degree in Medicine, Pharmacy, or Natural Sciences • Minimum 2 years of experience in Information Science within pharmaceutical research, development, or pharmacovigilance • Strong knowledge of biomedical literature databases, retrieval systems, and search languages • Ability to evaluate, interpret, and synthesize scientific data with analytical rigor • Excellent written and verbal communication skills in English, capable of presenting and discussing scientific results in international, cross-functional teams • Self-motivated, detail-oriented, and able to prioritize effectively in a dynamic environment If you are ready to contribute to cutting-edge literature analysis in pharmacovigilance and make a meaningful impact on patient safety, we look forward to receiving your application.

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