This postdoctoral position involves leading the preparation and analysis of skeletal muscle samples for proteomic and transcriptomic workflows, focusing on the 'dark proteome' in facioscapulohumeral muscular dystrophy (FSHD). The role combines technical leadership with broader involvement in translational research, collaborating with international partners.
The role involves leading projects to develop and benchmark AI models for predicting biological processes using genomic, multi-omic, and phenotypic data. The researcher will also contribute to statistical analysis, hypothesis testing, and preparing grant applications.
This role involves establishing and running iPSC-derived kidney and ureteric bud organoid models, using CRISPR interference to perturb candidate cis-regulatory elements, and profiling the consequences using advanced techniques like single-nucleus multiomics and CUT&RUN. You will work collaboratively with bioinformaticians and clinicians to generate and test hypotheses, and have opportunities for advanced training and independent research.
This role involves using ultra-long-read and hybrid sequencing technologies to explore highly repetitive DNA sequences in childhood cancer. You will develop laboratory protocols, produce sequencing data, and perform bioinformatic analysis with support from biostatisticians.
The role involves designing, building, and validating programmable nucleic-acid systems for genetic privacy. The postholder will work on developing molecular systems that can measure genetic information while limiting exposure of the underlying genomic sequence, engaging in iterative experimental and computational work.
This role involves researching the emergence of a multidrug-resistant fungal pathogen, Trichophyton indotineae, at the intersection of genomics, antimicrobial resistance, and molecular diagnostics. You will work in a multidisciplinary team to develop new diagnostic tools and contribute to clinical and public health efforts in East London.
The Clinical Development Medical Director is responsible for providing medical and scientific oversight for clinical trials, ensuring patient safety, and contributing to the design and execution of clinical studies. They will also participate in safety reviews, interact with healthcare professionals, and support regulatory activities.
The Clinical Development Medical Director is responsible for providing medical and scientific oversight for clinical trials, ensuring patient safety, and contributing to the design and execution of clinical studies. They will also participate in safety reviews, interact with healthcare professionals, and support regulatory activities.
This role leads the design and delivery of transformation-ready vectors and genome editing reagents for crop improvement programs, focusing on molecular construct development for gene editing and transgenic approaches in species like corn and wheat. The position establishes industrial-grade design standards, ensures technical robustness and regulatory alignment, and integrates with high-throughput transformation pipelines. It involves close collaboration with genotyping, automation, and commercial teams to enable scalable, traceable, and auditable vector development from concept to release.
This role leads the molecular confirmation and genotyping of gene-edited and transgenic crop events, ensuring high-quality, data-rich handover to downstream teams. The candidate will establish stage-gate criteria, manage genotyping workflows across multiple technologies, and integrate with transformation, bioinformatics, and trait discovery teams. The position is central to building a scalable, industrial-grade pipeline for crop development in species such as corn and wheat.
This role involves leading stem cell-focused drug discovery projects, developing and optimizing advanced stem cell-derived models, and integrating these models into client discovery programs. The position offers opportunities to work with cutting-edge technologies and collaborate with experts across various scientific disciplines.
This role involves applying and developing advanced machine learning and computer vision techniques to analyze multi-omic data and detect disease phenotypes. You will work closely with software engineers to translate research into practical tools, ensuring robustness and usability.
This role involves leading patient engagement initiatives in clinical research, ensuring patient perspectives shape clinical trial design and participant experiences. Responsibilities include advising study teams, building relationships with patient advocacy groups, and representing CSL externally to promote patient-centric research.
This role involves leading patient engagement initiatives in clinical research, ensuring patient perspectives shape clinical trial design, and building relationships with patient advocacy groups and healthcare institutions. The position requires significant experience in clinical research and patient engagement, with a focus on protocol development and site management.
The Associate Scientific Director will lead and oversee immunology and autoimmunity drug discovery projects, develop research strategies, and collaborate with cross-disciplinary teams. The role involves scientific leadership, ensuring research quality and compliance within a dynamic and innovative environment.
