For our client, a dynamic international biotechnology company focused on clinical-stage development, we recruit a:Senior/Executive Medical Director - Clinical
On behalf of our client, an international biotech company based in Baar, we are currently seeking a Senior Pharmacovigilance Scientist, Quality Document Manager. General Information:Start Date: ASAPDuration: 1 yearExtension: to be discussedContract Type: temporary contract via Randstad (employment)Location: Baar (ZG)Workload: 100%Tasks & Responsibilities: Perform QC Review of documents produced by SSA, including:Source data verification to ensure that all
Strategic Business Development & In-Licensing Specialist - 100%Starting date : ASAP Location : GenevaType of role : Permanent role Your ResponsibilitiesGenerate high-level scientific and commercial intelligence on potential licensors and therapeutic target areas.Manage business intelligence tools and databases (e.g., IMS, Evaluate Pharma) to support data-driven decision-making.Actively source, evaluate, and execute prioritized in-licensing