63 jobs for “Gene Therapy Scientist”
CSL Maidenhead
Acts as case management subject matter expert for assigned clinical trials, overseeing safety reporting plans, vendor performance and ICSR compliance. Leads pharmacovigilance processes, supports GxP inspections and audits, and provides study-specific training to vendors and internal teams. Requires deep PV and regulatory knowledge in a multinational pharmaceutical setting.
CSL Opfikon, Switzerland
Leads strategic sourcing and evaluation of late-stage external clinical assets in Immunology, from Phase 2 through marketed drugs. Sits on the Therapy Area Leadership Team, co-leads New Product Opportunity reviews, engages external KOLs and investigators, and drives cross-functional due diligence with BD to close deals.
Ellison Institute of Technology Oxford
Lead the development of a plant cell-based screening platform to evaluate carbon fixation, using quantitative methods and CRISPR-based genome editing in suspension cultures. Apply iterative design-build-test-learn cycles to identify improved photosynthesis enzyme variants and engineered pathways, advancing promising candidates into whole plants. Contribute to IP generation and collaborate across multidisciplinary teams.
Ellison Institute of Technology Oxford
Build and oversee plant growth and phenotyping facilities, ensuring controlled, reproducible environments in growth chambers and greenhouses. Hands-on player-coach role covering planting, irrigation, pollination, sampling and harvest, plus pest and pathogen management, GMO compliance and phenotype data capture. Also shapes field trial operations and future team hiring.
CSL Maidenhead
Leads strategic sourcing and evaluation of late-stage external clinical assets in Immunology, from Phase 2 through marketed drugs, as the senior S&E leader within the Therapy Area Leadership Team. Drives proactive sourcing, cross-functional due diligence, and KOL engagement, partnering with BD to advance high-priority opportunities through negotiation and deal close.
CSL Maidenhead US$317,000 – US$409,000 pa
Leads a cross-functional Clinical Development Team as the lead scientific expert, owning the clinical strategy, plan and medical monitoring for immunoglobulin programs. Accountable for clinical content of regulatory submissions and study documents, and serves as medical monitor across trials in a matrixed environment.
CSL Opfikon, Switzerland US$317,000 – US$409,000 pa
Leads the cross-functional Clinical Development Team as lead scientific expert, owning the Clinical Development Plan and integrating internal and external contributions into program strategy. Serves as medical monitor, authors key regulatory and study documents, and presents to safety and review committees.
CSL Maidenhead
Provides medical and scientific expertise on clinical safety across the full product lifecycle, with emphasis on evaluating safety data during clinical development and post-approval. Chairs the Safety Management Team, oversees signal detection, aggregate reports (DSURs, PSURs, RMPs) and regulatory responses, and sets safety strategy for global cross-functional development and post-marketing teams.
CSL Opfikon, Switzerland
Provides medical and scientific expertise on clinical safety across a product's lifecycle, with emphasis on signal detection, risk management and regulatory submissions. Chairs the Safety Management Team, oversees aggregate reports such as DSURs, PSURs and RMPs, and acts as the safety representative in cross-functional development and post-marketing teams.
