Senior Data Scientist — Literature
Vollzeit @Albedis veröffentlicht 5 Tagen agoJob-Beschreibung
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.
