26 jobs for “Protein Engineer”
Ellison Institute of Technology Oxford £40,000 pa
Develops generative protein design models that capture enzyme dynamics and function, designing conformationally dynamic catalysts. Runs computational and statistical analyses, publishes findings, and collaborates with in vivo evolution teams across the institute. Also mentors PhD students and research assistants and pursues translational and IP opportunities.
Ellison Institute of Technology Oxford
Design and conduct experiments on nanopore technologies, single-molecule analysis, and 3D tissue engineering, spanning chemistry, biology, physics and engineering. Postdocs lead development of emerging biotech methods, publish impactful research, and mentor junior researchers within a 100+ researcher institute.
CSL Breda, Netherlands US$212,000 – US$251,000 pa
Leads the full scope of statistical contribution to a clinical development programme, defining statistical strategy and methodologies for trial design, analysis and regulatory submissions. Represents Biostatistics in interactions with authorities such as FDA, EMA and PMDA, and manages outsourcing or internal statistical programmers. Two positions support multiple therapeutic areas.
CSL Opfikon, Switzerland US$212,000 – US$251,000 pa
Leads the full statistical contribution to a clinical development programme, defining statistical strategy for trial design, analysis and regulatory submissions, and representing Biostatistics in interactions with the FDA, EMA and PMDA. Also manages outsourcing to CROs and internal statistical programmers, and supports departmental improvement initiatives.
Vertex Pharmaceuticals Oxford
A 12-month laboratory-based industrial placement within the Structural Biology & Biophysics department, working at the interface with Biology on a collaborative project. The role involves membrane protein preparation and reconstitution into lipid-based model systems, functional characterisation using electrophysiology, and interpreting biochemical and biophysical data to support early drug discovery.
CSL Maidenhead
Leads strategic sourcing and evaluation of external innovation opportunities in Haematology, identifying preclinical to Phase 1 assets and shaping early partnering strategies. Sits on the Therapeutic Area Leadership Team, co-leads New Product Opportunity reviews, drives cross-functional due diligence and works with Business Development on deal execution. Hybrid, three days a week at an R&D hub site.
CSL Opfikon, Switzerland
Leads strategic sourcing and evaluation of external innovation opportunities in Haematology, identifying preclinical to Phase 1 assets and shaping early partnering strategies. Sits on the Therapeutic Area Leadership Team, co-leads New Product Opportunity reviews, drives cross-functional due diligence, and works with Business Development on deal execution. Hybrid, three days a week at an R&D hub site.
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.
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
The Senior Medical Director, Global Clinical Program Lead is responsible for the strategic leadership of the Clinical Development Team, ensuring the design and execution of clinical strategies for immunoglobulin medicines. Key responsibilities include leading cross-functional teams, maintaining alignment with stakeholders, and ensuring compliance with regulatory standards.
CSL Opfikon, Switzerland
The Senior Medical Director, Global Clinical Program Lead is responsible for the strategic leadership of clinical development programs, including team leadership, clinical oversight, and document authorship. The role involves cross-functional collaboration, regulatory interactions, and ensuring high scientific standards.
