senior data scientist - literature (m/f/d).

• Start date: ASAP
• Duration: 9 months (maternity cover)
• Contract: temporary contract via Randstad
• Extension: to be discussed
• Workplace: Basel 
• Workload: 100%
• Home Office: possible
• Working hours: Standard

Tasks & Responsibilities:
 

• Performs ad-hoc literature searches in biomedical databases to identify adverse drug reactions and risks in association with company’s medicinal products and devices.
• Develops, tests, documents and maintains literature search profiles to identify published case reports of adverse drug reactions in association with company’s medicinal products.
• Develops, tests, documents and maintains search profiles to identify adverse drug reactions and risks in association with company’s medicinal products for the following purposes: Development Safety Update Reports (DSURs), Periodic Benefit-Risk Evaluation Reports (PBRERs) and signal detection.
• Develops, tests, documents and maintains search profiles to identify incidents and risks in association with company’s medical devices for the following purposes: Medical Device Incident Reports (MDIR) and signal detection.
• Performs efficacy searches in biomedical databases for PDMA to identify the efficacy of company’s medicinal products for the following purposes: Periodic Safety Update Reports (PBRER).
• Maintains effective relationship with customers in PDS and beyond Interacts with customers to define the search criteria for literature searches.
• Checking the results of literature searches for plausibility.
• Ensure timely and correct delivery of search results.
• Performs literature searches in compliance with Standard Operating Procedures.
• Acts as core member in Safety Literature Group, active contribution to knowledge sharing.
• Creates training material for team members and stakeholders on retrieval and reporting related topics and delivers the training.
• Proactively raise ideas and identify opportunities to enhance ways of working (including processes, methods, technologies etc.). and share best practices and lessons learned with peers.
• Establish, promote and maintain effective working relationships with other stakeholders, departments and functions as required.
• Ensures any issues relating to literature searches are adequately addressed at the lowest level and escalated appropriately.

• M.S. or University degree in medicine, pharmacy or natural sciences.
• Min. 2 years experience in Information Science and solid pharmaceutical experience in research, development or research informatics, including experience in Pharmacovigilance
• Good knowledge of medicine and drug development
• Good knowledge of external and internal biomedical and drug literature databases as well as the corresponding retrieval systems and languages
• Ability to evaluate, interpret and synthesize scientific data (analytical thinking)
• Excellent written and verbal communication skills and ability to present and critically discuss scientific data in discussions
• Classical text searching capabilities
• Expertise in literature sources and databases both, internal and external (e.g. Competitor Information Access Platform; DIALOG)
• Ability to build strong working relationships with appropriate personnel in other functional groups within and outside of the Safety Risk Management (PDS) organization.
• Strong communication skills in an international cross-functional environment with the ability to effectively explain search strategies, both verbally and in writing
• Excellent written and verbal communication skills and ability to present and critically discuss scientific data in discussions
• Team player with ability to function in a multi-disciplinary environment
• Self –motivated, able to prioritize and plan effectively
• Good attention to detail
• Fluent in English (verbal and written)