Senior Data Scientist - Literature; LSW - BS
4040, Basel, Kanton Basel-Landschaft, Switzerland
Listed on 2026-01-01
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Healthcare
Data Scientist, Medical Science, Clinical Research
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We are looking for a Senior Data Scientist - Literature (m / f / d) (LSW) - BS
BackgroundThe position of Senior Data Scientist – Literature sits within the Safety Analytics and Reporting (SAR) group of the Safety Risk Management (PDS) function. In this role, you support Roche’s product portfolio by conducting global literature searches and extracting information from biomedical databases to address safety-related medical inquiries for both medicinal products and medical devices.
Additionally, the team provides tailored literature searches for various Pharma Development (PD) groups, including Medical Affairs , to gather evidence on product efficacy for documents such as Periodic Safety Update Reports (PBRERs) . As many of these deliverables are mandated by health authorities, the role requires consistent quality, adherence to timelines, and close alignment with stakeholders from Clinical Science, Safety Operations, PDMA, Regulatory Affairs and related functions.
The insights generated from these analyses form a crucial component of patient-focused risk assessment. You will further contribute by supporting projects, improving processes, and participating in strategic initiatives that strengthen Roche’s safety strategy.
The Ideal CandidateThe preferred candidate holds a university degree in medicine, pharmacy or life sciences and brings at least two years of experience in Information Science , ideally with strong exposure to pharmacovigilance and drug development.
We are looking for a proactive, analytical and collaborative individual with excellent communication skills and the ability to train others. Strong organisational skills, a continuous improvement mindset and the ability to build effective cross-functional relationships are essential for success in this role.
General InformationStart date : asap
Latest start date : 01 February 2026
Planned duration : 9 months (maternity cover)
Extension : TBD
Workplace :
Basel
Workload : 100%
Home Office : yes
Travel required : no
Team size : 2 people
Department : PV & Scientific Development (TLSC)
Working hours :
Standard
- Conduct ad-hoc literature searches in biomedical databases to identify potential adverse drug reactions and safety risks associated with the company’s medicinal products and devices.
- Develop, test, document and maintain literature search profiles for published case reports of adverse drug reactions.
- Create and maintain search strategies supporting regulatory deliverables such as Development Safety Update Reports (DSURs) , Periodic Benefit-Risk Evaluation Reports (PBRERs) and signal detection activities.
- Build and maintain search profiles for identifying incidents and safety risks related to medical devices (e.g., MDIR, signal detection).
- Perform efficacy-focused literature searches for PDMA to support PBRER preparation.
- Collaborate with internal stakeholders to define search criteria and clarify requirements.
- Review search results for accuracy, plausibility and completeness.
- Ensure timely, compliant and well-documented delivery of literature search outputs.
- Actively contribute to the Safety Literature Group and support knowledge-sharing activities.
- Develop training materials on literature retrieval and reporting topics and deliver training sessions to colleagues and stakeholders.
- Identify improvement opportunities related to processes, methods and tools and share best practices within the team.
- Establish and maintain strong working relationships with other Roche functions and departments.
- Ensure that issues related to literature searches are addressed promptly and escalated when necessary.
- University degree (medicine, pharmacy or natural sciences).
- Minimum 2…
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