Sr. Scientist, Drug Safety (Pharmacovigilance)

Centessa Pharmaceuticals plc (Nasdaq: CNTA) new kind of pharmaceutical company with a deconstructed R&amp;D environment that prioritizes data driven decision making led by subject matter experts. Centessa is advancing a portfolio of high conviction programs with strong biological validation. Our asset-centric model offers a unique R&amp;D logic that has been applied by single asset companies to improve productivity. This operating model has minimal centralized infrastructure, reduced hierarchy, and exclusive focus on data driven capital allocation. Our teams are uniquely incentivized to expeditiously interrogate key scientific hypotheses. We believe the asset-centric model can lead to improved success rates for programs with greater speed and modest costs. &nbsp; Description of Role We are seeking a &nbsp;Senior &nbsp;Scientist, Drug Safety (Pharmacovigilance) to support pharmacovigilance activities across&nbsp; Centessa’s &nbsp;clinical-stage development programs. Reporting&nbsp; to&nbsp; Centessa’s &nbsp; Head of Safety and Pharmacovigilance, &nbsp;this role will contribute to the review and analysis of safety data to support ongoing safety surveillance, regulatory compliance, and program execution. The&nbsp; Senior&nbsp; Scientist will work closely with cross-functional partners and external vendors to ensure high-quality safety deliverables and&nbsp; maintain &nbsp;inspection-ready pharmacovigilance processes in a fast-paced, development-focused environment. &nbsp; Key Responsibilities Provide advanced scientific oversight of ICSR and clinical trial SAE evaluation, ensuring medical accuracy, regulatory reportability, and consistency across global development programs.&nbsp; <li data-leveltext="" data-font=&