Associate Safety Director (m/f/d)

Description du poste

For a leading pharmaceutical company, we are looking for a qualified General Information: Location: Basel Workload: 100% Start: 21.08.2026 Duration: 12 months (Extension possible) Home Office: First 3 months full on-site presence for training; afterwards, max. 40% Your Responsibilities: Own and maintain an expert understanding of the safety profile of assigned product(s)/therapy area(s) and their strategic context (disease, MoA, competitors). Lead case management and reporting activities: medical review of ICSRs and aggregate reports (e.g., DSUR, PBRER). Drive signal detection and signal management, including safety assessments and responses to Health Authority requests (incl. quality-related safety topics). Contribute to and help shape the product safety strategy, including benefit–risk considerations. Independently manage risk management deliverables (e.g., RMP, CCDS, labeling/IB updates and risk communications). Review key clinical documents (protocols, study reports, IB, ICF) to ensure alignment with the safety strategy and appropriate risk communication. Provide safety-science input to regulatory submissions and governance/oversight forums (e.g., IND/NDA/MAA activities, iDMC/IMC, DSC/DRC), collaborating with SSLs, teams, and vendors. Your Profile: Qualified healthcare professional or Life Sciences graduate (postgraduate degree such as PhD/MSc/PharmD is an advantage). More than 4 years drug development experience (pharma or related industry). More than 3 years in drug safety/pharmacovigilance (or closely related field). Minimum candidate level required: Associate Safety Director. Strong Excel/Word/PowerPoint skills; able to extract data from safety databases and apply complex data analysis. Fluent English (written and spoken) Interested? Then apply today. We look forward to hearing from you!