Lead global respiratory epidemiology and real-world evidence initiatives to inform vaccine development, designing and delivering studies on disease burden, treatment patterns, and safety. Partner with cross-functional teams and external collaborators to generate regulatory-grade evidence and shape development strategies. Drive scientific dissemination through publications, regulatory submissions, and international conferences.
Leads global respiratory epidemiology and real-world evidence initiatives to inform vaccine development, designing and delivering studies on disease burden, treatment patterns, and safety. Works cross-functionally with clinical, regulatory, and safety teams, manages external collaborations, and drives scientific dissemination through publications and regulatory submissions. Focuses on strategic epidemiological planning and mentoring junior staff within a matrixed R&D environment.
This 12-month industrial placement involves supporting the development of pharmaceutical drugs through analytical chemistry techniques such as HPLC, GC-MS, NMR, and XRPD. You'll work within a collaborative team to deliver analytical data that supports drug development timelines, adhering to GMP and GLP standards while gaining hands-on experience in a regulated environment.
Lead the development and execution of bioanalytical strategies for a diverse portfolio of AI-designed therapeutics, including small molecules, biologics, and ADCs. Design and validate PK, PD, and immunogenicity assays, manage global CROs, and integrate bioanalytical data into AI models to refine drug discovery. Play a key role in IND-enabling studies and cross-functional preclinical development in a hybrid London-based role.
Lead clinical pharmacology strategy for small molecule programs in oncology and non-oncology areas, designing and executing studies from Phase 1 through late development. Utilize AI-driven models for PK/PD prediction, dose optimization, and regulatory submissions, while managing CROs and translating preclinical data into human dosing strategies.
This role focuses on enabling secure and compliant cross-border data transfers for AstraZeneca’s Beijing AI Center, primarily from global R&D into China. The scientist will lead first-pass triage, provenance tracing, metadata coordination, and evidence preparation for data sharing requests, ensuring alignment with regulatory requirements like DOJ EO 14117 and internal governance. It bridges scientific data, compliance, and operational execution to accelerate AI-driven drug discovery while maintaining audit readiness and building scalable processes.
This role involves leading clinical strategy and execution for cardiovascular/stroke medicine programs, with responsibility for trial design, regulatory documentation, and cross-functional collaboration. The Senior Clinical Development Medical Director will guide global teams, interpret complex clinical data, and contribute to safety and development decisions across the drug lifecycle. Expertise in anticoagulation and outcome trials is key, along with strong leadership in a matrix environment.
This role involves leading early-phase clinical development (Phase 1 and 2) of novel gastroenterology therapies, with a focus on inflammatory bowel disease (IBD). The Translational Medicine Expert will design clinical development plans, serve as medical lead for trials, and collaborate closely with research, biomarker, and late-phase development teams. The position requires strong scientific leadership, engagement with key opinion leaders, and active involvement in regulatory interactions.
This role involves designing and executing experiments in synthetic chromosome engineering, with a focus on centromere design, mitotic segregation, and meiotic control in mammals and plants. The researcher will develop novel methodologies, analyse genomic datasets, and contribute to foundational work in programmable synthesis of large genetic systems. Collaboration, publication, and mentoring are key components, within a multidisciplinary team advancing the engineering of biology.
Leads an independent research group focused on advancing the engineering of biology, with a focus on genome synthesis and functional DNA design. Works collaboratively within a multidisciplinary institute to pioneer transformative applications in health, agriculture, and clean energy. Involves mentoring early-career researchers, shaping cutting-edge facilities, and driving long-term, scalable biological solutions.
Lead the strategic sourcing and evaluation of late-stage therapeutic assets in Immunology, Hematology, or related areas, from Phase 2 through marketed drugs. Drive cross-functional due diligence, engage with key opinion leaders and clinical networks, and shape portfolio strategy through high-impact partnerships and transactions. Operate within a global biotech ecosystem with strong collaboration across R&D, BD, and regulatory functions.
This role involves leading CSL's presence in key innovation hubs across Northern Europe and the UK, building strategic relationships with biotech, academia, and investment networks. The Director will source and evaluate opportunities, lead deal teams, and represent CSL at industry events to enhance the company's reputation and deal flow.
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 role involves leading global clinical strategy for Roche’s toxicology and drug testing portfolio, including advanced diagnostic platforms like the cobas i601. The Clinical Development Lead will design and execute high-impact clinical programs, engage with regulatory authorities, integrate real-world evidence, and collaborate with key opinion leaders to drive diagnostic innovation and ensure scientific validity across global markets.
Operate within a GMP-regulated warehouse environment at Moderna’s Harwell site, managing inbound and outbound material flows, inventory control via SAP, and supporting continuous mRNA manufacturing operations. Perform cycle counts, documentation, and logistics coordination while adhering to strict quality and safety standards. Gain exposure to digital-first and AI-enabled tools within a fast-paced, collaborative pharmaceutical setting.
