Senior Data Scientist (m / f / d)
Freelance / temporary employment for a project Basel Stadt Start date : asap Reference number : 853098 / 1
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Responsibilities
- Perform ad-hoc literature searches in biomedical databases to identify adverse drug reactions and risks
- Develop, test, document, and maintain search profiles for published case reports and safety updates
- Create and manage search profiles for Development Safety Update Reports (DSURs), PBRERs, and signal detection
- Build search profiles to identify incidents and risks in association with medical devices (MDIRs, signal detection)
- Conduct efficacy searches in biomedical databases to support safety and medical affairs reporting
- Collaborate with stakeholders to define search criteria and ensure plausibility of results
- Deliver timely and compliant search results in line with SOPs and regulatory requirements
- Contribute to the Safety Literature Group, knowledge sharing, training, and process improvements
Profile
or university degree in medicine, pharmacy, or natural sciencesSolid experience in Information Science with pharmaceutical research or development backgroundSolid experience in Pharmacovigilance and drug development processesStrong knowledge of biomedical and drug literature databases, retrieval systems, and search languagesAbility to evaluate, interpret, and synthesize scientific data with analytical precisionExpertise in internal and external literature sources and databases (, DIALOG, competitor platforms)Excellent written and verbal communication skills, with ability to present and critically discuss dataTeam-oriented, self-motivated, detail-focused, with strong planning and prioritization skills; fluent in EnglishBenefits
Opportunity to contribute directly to patient-focused risk management and regulatory safety deliverablesCollaborative, cross-functional environment with international exposureProfessional growth through involvement in strategic initiatives, training, and process innovation