Leads external innovation sourcing and evaluation in Haematology, identifying preclinical to Phase 1 assets, driving due diligence, and shaping early partnering strategies. Works within the Therapeutic Area Leadership Team to advance high-potential opportunities and collaborates with Business Development to execute deals. Engages with biotech, academia, and investors to build a robust pipeline.
Leads strategic sourcing and evaluation of early-stage innovation in haematology, from preclinical to Phase 1 assets. Drives due diligence, shapes partnering strategies, and executes transactions in collaboration with Business Development. Embedded in the Therapeutic Area Leadership Team to influence portfolio planning and external innovation priorities.
The Team Coordinator supports the President Team by ensuring seamless day-to-day operations, executive meeting readiness, and high-quality guest experiences. This role handles physical logistics for events, internal speaking engagements, and offsites, acting as the on-the-ground point of contact for high-profile visitors and external facilitators. The position requires meticulous attention to detail, proactive problem-solving, and close coordination with internal and external stakeholders to maintain flawless executive suite operations.
Lead DMPK strategy for drug discovery projects using an AI-first approach, integrating quantitative pharmacology and ADME data to guide candidate selection. Collaborate with chemistry, pharmacology, and machine learning teams to optimise molecule design and advance predictive models. Contribute to regulatory documentation and drive innovation in human PK prediction and biotransformation understanding.
This role involves leading the creation and management of investigator site budgets and contracts for clinical trials, using Grants Manager and FMV benchmarking tools. The candidate will oversee CRO activities, ensure budget consistency across trials, and support timely site activation by managing negotiations and identifying risks. Collaboration with legal, clinical operations, and external partners is central to ensuring compliance and efficiency in contract execution.
This role involves developing, validating, and executing ligand-binding and cell-based assays to support mRNA medicine development. The candidate will generate pharmacodynamic and immunogenicity data in a regulated GcLP environment, manage critical reagent characterization, and contribute to clinical sample testing using Watson LIMS. The position emphasizes scientific rigor, regulatory compliance, and collaboration within a high-performance team advancing novel bioanalytical assays.
This role involves leading and supporting the operational strategy and delivery for complex oncology clinical trials, coordinating cross-functional inputs, and maintaining inspection readiness. The position offers opportunities for growth and influence over program strategy.
This role involves performing targeted and non-targeted trace analysis of small and large molecules using mass spectrometry, developing sample preparation methods, and leading analytical projects from sample preparation to data interpretation and reporting. The position is hands-on and lab-based, with a focus on extractables and leachables, and includes contributing to regulatory submissions and overseeing work at CROs.
The Executive Director, Asset Team Lead, will drive the strategic positioning of clinical assets in oncology and immunology, leveraging Recursion's proprietary OS and ClinTech insights. This role involves cross-functional collaboration to ensure the advancement of transformative medicines, with a focus on competitive positioning and patient benefit.
This role involves leading the end-to-end clinical supply chain strategy for global trials, managing demand forecasting, packaging, labeling, distribution, and inventory. You will work closely with cross-functional teams to ensure supply strategies align with trial milestones and commercial readiness, leveraging AI and advanced tools to optimize processes.
This role leads global clinical strategy for Roche’s toxicology and drug testing portfolio, driving clinical development programs from concept to registration. The Clinical Development Leader will design evidence generation plans, engage with regulatory authorities, integrate real-world data, and collaborate with KOLs to advance diagnostic solutions. They will also mentor team members and shape scientific communication to support product adoption and innovation in clinical toxicology.
Leads global clinical strategy for Roche’s toxicology and drug testing portfolio, designing and executing clinical development programs to support regulatory approval and market adoption. Acts as scientific authority in interactions with health agencies, drives real-world evidence integration, and collaborates with KOLs and cross-functional teams to advance diagnostic innovation. Focuses on generating robust clinical evidence to demonstrate safety, effectiveness, and scientific validity of diagnostic solutions.
This PhD studentship focuses on developing dynamic DNA data structures for molecular information storage and computing, combining computational design with experimental lab work. The project builds on pioneering research in DNA-based stack structures and aims to create novel molecular data structures such as queues, deques, and priority structures. The candidate will work within an interdisciplinary team, designing, modelling, and validating DNA/RNA systems and molecular circuits for in vitro or cellular applications.
This role involves leading complex clinical technology transformation and data migration initiatives across the clinical trial ecosystem. Responsibilities include managing end-to-end migration programmes, data validation, and ensuring compliance with regulatory requirements. The role also involves collaborating with global stakeholders to deliver scalable and compliant technology solutions.
As a Quality Specialist, you will support the maintenance and continuous improvement of the Quality Management System (QMS) in a highly regulated pharmaceutical environment. Your responsibilities will include managing deviations, CAPAs, change controls, and complaints, as well as supporting audit and inspection readiness activities. You will collaborate with cross-functional teams to ensure quality objectives are met.
