Latest regulatory affairs Jobs

Head, Oncology Clinical Development - ADCs

Leads the end-to-end clinical development of an antibody-drug conjugate (ADC) oncology asset across multiple tumor types, from first-in-human through registrational trials and launch readiness. Responsible for shaping clinical strategy, overseeing global trials, engaging with regulatory authorities, and leading cross-functional teams in a matrixed environment. Involves governance leadership, scientific advisory boards, and integration of innovative approaches such as AI/ML and real-world evidence to accelerate development.

GSK US$242,250 – US$403,750 pa

Head, Oncology Clinical Development - ADCs

Leads end-to-end clinical development of an antibody-drug conjugate (ADC) oncology asset across multiple tumor types, from first-in-human through registrational trials and market launch. Drives integrated clinical strategy, translational research, regulatory submissions, and cross-functional collaboration across global teams. Engages with governance bodies, scientific advisory boards, and external experts to shape development and competitive positioning.

GSK US$242,250 – US$403,750 pa

Associate Director, CMC Regulatory Science, International

This role involves leading CMC regulatory strategy for global mRNA product development, preparing and reviewing regulatory submissions, and guiding cross-functional teams on compliance and agency interactions. The position requires deep expertise in biologics CMC regulations, particularly in EU and ROW markets, and plays a key part in shaping regulatory pathways across vaccines, oncology, and rare diseases. Based at the Harwell site, it emphasizes in-office collaboration within a multidisciplinary team.

Moderna

On-site Permanent

Central Monitor (Data Surveillance Lead)

The Central Monitor (CM) oversees and supports clinical trials through centralized monitoring activities, ensuring data quality, identifying risks, and enhancing trial oversight. They collaborate with cross-functional teams, configure Central Monitoring technology, and provide ongoing data surveillance and risk management.

Novartis London, United Kingdom

Central Monitor (Data Surveillance Lead)

The Central Monitor (CM) oversees and supports clinical trials through centralized monitoring activities, ensuring data quality, identifying risks, and enhancing trial oversight. They collaborate with cross-functional teams, configure Central Monitoring technology, and provide ongoing data surveillance and risk management.

Novartis Ardross, Alba / Scotland, IV17 0YF, United Kingdom

Sr. Research Associate, Bioanalytical & Molecular Assays - Ligand Binding Assays

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.

Moderna Oxford, United Kingdom

Hybrid Permanent

Director, Search & Evaluation Early TA Lead (Haem)

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.

CSL

Director, Search & Evaluation Early TA Lead (Haem)

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.

CSL

Associate Director, Clinical Supply Chain, Cambridge, MA

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.

Isomorphic Labs Cambridge, United Kingdom

Field Service Engineer - Medical Diagnostics - North Region - Liverpool - Scotland

This role involves providing on-site and remote technical support for Roche’s diagnostic systems, including troubleshooting electro-mechanical faults, performing preventive maintenance, and delivering customer training. The engineer ensures high system uptime and regulatory compliance across customer sites in the North Region, from Liverpool to Scotland. The position emphasizes technical excellence, customer engagement, and collaboration within a field support team.

Roche United Kingdom

Scientist, Plant Biology and Functional Genomics - Plant Biology Institute

This role involves conducting high-impact research in plant biology and functional genomics, focusing on genetic targets and engineering strategies to modify plant cell growth, division, and morphology. The scientist will work closely with AI, molecular engineering, and plant transformation teams to translate biological hypotheses into testable genetic perturbations and guide the interpretation of resulting phenotypes.

Ellison Institute of Technology Oxford, United Kingdom

On-site Permanent

Vector Design Lead - Plant Biology Institute

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.

Ellison Institute of Technology Oxford, United Kingdom

On-site Permanent

Lecturer in Biomedical Science (Blood Sciences) - Teaching & Scholarship)

The role involves teaching, assessing, and developing the curriculum in Biomedical Science, specifically in Blood Sciences. You will also support students, engage in scholarly activities, and collaborate with external partners and regulatory bodies.

London South Bank University London, United Kingdom £42 – £50 pa

Permanent

Undergraduate Clinical Development Scientist

This role involves supporting the clinical development of vaccines through various activities, including protocol development, regulatory compliance, data review, and medical oversight. The position provides hands-on experience in a busy clinical research environment, contributing to global vaccine programs and promoting STEM activities.

Pfizer Marlow, United Kingdom

Senior Scientist - ELN & Data Specialist, Global Technical Development

This role involves hands-on administration, configuration, and continuous improvement of an Electronic Lab Notebook (ELN) platform to support R&D and Technical Development laboratories. The scientist will define ELN standards, design workflows and templates, integrate systems, and develop data repositories to enable data-driven decision-making. Collaboration with cross-functional teams is essential to ensure compliance, data integrity, and effective use of the ELN across scientific operations.

Orchard Therapeutics London, United Kingdom

Hybrid Permanent