The Principal Scientist role involves integrating deep expertise in computational and statistical methods to analyze large-scale genetic data, identify causal gene-phenotype links, and guide drug discovery and development. The role requires collaboration with multidisciplinary teams and staying informed about recent research in the field.
This role involves leading medical oversight in gastrointestinal (GI) oncology clinical development, ensuring patient safety and clinical integrity across study design, execution, and data interpretation. The Medical Director collaborates with cross-functional teams to integrate physician insights into clinical trials, engages with external experts and regulators, and contributes to regulatory submissions and scientific communications. The position requires deep expertise in oncology and clinical development within a global pharmaceutical environment.
Lead the technical development and implementation of a new labeling and secondary packaging operation at Moderna’s Harwell site, from initial design through commissioning and validation. Establish maintenance strategies, ensure GMP compliance, and drive continuous improvement using engineering excellence principles and digital tools. Build and lead a high-performing engineering team to support long-term operational success in a regulated biotech environment.
This role involves performing high-quality analytical chemistry and stability testing, supporting manufacturing processes, and maintaining GMP compliance. You will work with advanced analytical technologies and laboratory information systems to ensure the quality and integrity of mRNA materials and products.
This role involves leading end-to-end clinical trial material planning, vendor management, packaging, labeling, inventory management, and global distribution. You will work closely with Clinical Operations and the Clinical Development team to ensure seamless clinical trial execution and compliance with regulatory standards.
This is a general interest application for roles at Isomorphic Labs, an AI-driven drug discovery company. Candidates may be considered for positions including Software Engineers, ML Researchers, Computational Chemists, and Technical Project Managers. The role involves interdisciplinary collaboration to advance AI models for rational drug design and digital biology, within a culture emphasising curiosity, bravery, determination, and teamwork.
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.
Develop and lead a plant cell-based screening platform to evaluate carbon fixation and photosynthetic efficiency, using suspension cultures and genetic engineering techniques like CRISPR. Identify improved enzyme variants and metabolic pathways, then validate top candidates in whole plants to enhance crop performance. Work within a multidisciplinary team to drive discovery from lab to scalable agricultural solutions, with strong emphasis on IP generation and ethical innovation.
This role involves serving as the physician lead within an oncology clinical development team, providing medical expertise in study design, safety oversight, and data interpretation for gastrointestinal (GI) cancer trials. The Medical Director ensures patient safety and clinical integrity across clinical studies, collaborates with cross-functional teams and external experts, and contributes to regulatory submissions and scientific communications. The position supports GSK’s mission to advance innovative cancer treatments grounded in disease biology and real-world impact.
The Medical Director, Oncology Clinical Development - GI, provides medical expertise and oversight for clinical studies, ensuring patient safety and clinical integrity. The role involves leading medical monitoring, interpreting clinical data, and collaborating with cross-functional teams to advance oncology treatments.
This role involves leading medical monitoring and safety oversight for gastrointestinal (GI) oncology clinical trials within GSK’s global development programme. The Medical Director provides physician-level expertise in study design, data interpretation, and regulatory engagement, ensuring patient safety and clinical integrity across phases I–III. Working within a cross-functional matrix team, the role integrates medical insight into clinical strategy and collaborates with external experts and investigators to advance innovative cancer therapies.
The Medical Director, Oncology Clinical Development is responsible for providing medical expertise in the design, conduct, and interpretation of clinical studies for lung and head/neck cancers. Key responsibilities include medical monitoring, safety oversight, protocol development, and collaboration with cross-functional teams and external experts.
The Medical Director, Oncology Clinical Development is responsible for providing medical expertise in the design, conduct, and interpretation of clinical studies for lung and head/neck cancers. This role involves leading medical monitoring, ensuring patient safety, and collaborating with cross-functional teams to integrate medical considerations into study execution and regulatory interactions.
The Medical Director, Oncology Clinical Development role involves leading medical monitoring, safety oversight, and clinical data interpretation for clinical studies in lung and head/neck cancers. The role requires strong clinical expertise, collaboration with cross-functional teams, and engagement with external experts to ensure patient safety and study integrity.
The Medical Director, Oncology Clinical Development is responsible for providing medical expertise in the design, conduct, and interpretation of clinical studies for lung and head/neck cancers. Key responsibilities include medical monitoring, safety oversight, and collaboration with cross-functional teams to ensure patient safety and clinical integrity.
