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Senior data scientist - literature

Liestal
ALBEDIS
Data Scientist
EUR 100’000 - EUR 125’000 pro Jahr
Inserat online seit: 11 Dezember
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.

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