Senior Data Scientist - Literature

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

• 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

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.