Latest regulatory affairs Jobs

Director, Oncology Translational Medicine

Lead the development and execution of biomarker and translational medicine strategies for late-stage oncology assets, integrating cutting-edge technologies to identify predictive biomarkers and optimise clinical decision-making. Collaborate across functions to align biomarker strategies with clinical development plans and support patient segmentation, dose selection, and regulatory strategies. Drive scientific innovation through real-world data, multi-omic analyses, and external partnerships to advance GSK’s oncology pipeline.

GSK US$189,750 – US$316,250 pa

Medical Director Clinical Development- Respiratory

This role involves leading clinical development for respiratory assets within GSK’s Respiratory, Immunology & Inflammation Research Unit. The Medical Director will design and deliver clinical and translational strategies, oversee study execution, ensure patient safety, and contribute to regulatory submissions. Working cross-functionally, they will help shape development plans that align with scientific innovation and patient needs, particularly in pulmonary hypertension and related areas.

GSK £222,750 – £371,250 pa

Director, Resilience Lifecycle & Supply Chain Operations

Leads end-to-end product lifecycle management and supply chain operations across the UK, Canada, and Australia, aligning global strategies with local execution. Focuses on launch planning, supply chain resilience, cross-market coordination, and operational governance. Drives standardization, crisis preparedness, and continuous improvement through cross-functional leadership and digital transformation initiatives.

Moderna United States US$167,000 – US$300,700 pa

Director, Resilience Lifecycle & Supply Chain Operations

Leads end-to-end product lifecycle management, launch planning, and supply chain operations across the UK, Canada, and Australia, ensuring alignment between global strategy and local execution. Establishes governance, performance standards, and escalation frameworks while driving operational resilience, compliance, and cross-market collaboration. Focuses on S&OP, business continuity, crisis preparedness, and digital transformation through analytics and automation.

Moderna

Clinical Development Medical Director - Neuromuscular

Leads global clinical development programs in neuroscience, with a focus on neuromuscular or related disorders. Provides medical and scientific leadership across trial design, regulatory submissions, and data interpretation. Engages with regulatory bodies and key opinion leaders to shape clinical strategy and advance innovative therapies.

Novartis Ardross, Alba / Scotland, IV17 0YF, United Kingdom £83,510 – £155,090 pa

Hybrid Permanent

Clinical Development Medical Director - Neuromuscular

Leads global clinical development programs in neuroscience, with a focus on neuromuscular or related disorders. Provides medical and scientific leadership across trial design, regulatory submissions, data interpretation, and external engagement. Works cross-functionally to drive innovative therapies from concept to approval, with emphasis on gene therapy and complex clinical data.

Novartis Ireland €90,300 – €167,700 pa

Hybrid Permanent

Global Development Lead, Internal Medicine, Sr. Director (MD)

This role involves leading clinical development for Internal Medicine assets within Pfizer's Research & Development division, with accountability for designing, executing, and interpreting global clinical studies to support regulatory submissions. The individual will act as a key clinical leader, collaborating with cross-functional teams and external stakeholders to shape clinical development plans, trial design, and lifecycle strategies. Expertise in obesity, endocrinology, or chronic weight management is required, along with leadership in managing large-scale clinical programs and regulatory deliverables.

Pfizer £274,500 – £457,500 pa

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (MD)

This role leads clinical development for Internal Medicine assets within Pfizer's Research & Development division, serving as the primary clinical accountable leader for global drug development programs. The position involves end-to-end responsibility for clinical strategy, trial design, regulatory submissions, and cross-functional team leadership across a complex matrix environment. It also includes engagement with external stakeholders, patient advocacy groups, and oversight of safety and lifecycle planning, with a focus on obesity and related therapeutic areas.

Pfizer £274,500 – £457,500 pa

On-site Permanent

Senior Scientist – Diagnostic Deployment

This role involves hands-on development, optimisation, and validation of tissue-based diagnostic assays, primarily using histology and immunohistochemistry (IHC), to support AstraZeneca's clinical trials. The scientist will integrate digital and computational pathology tools, ensure compliance with regulatory standards like CAP/CLIA and ISO, and enhance laboratory workflows through LIMS integration. The position emphasizes scientific rigour, cross-functional collaboration, and innovation in oncology diagnostics.

AstraZeneca Cambridge, United Kingdom

Senior Quality Associate – Accredited Diagnostic Development Laboratory

This role involves leading quality management within AstraZeneca’s accredited internal diagnostic laboratory, ensuring compliance with CAP/CLIA, IVDR, and ISO standards during the development and validation of precision diagnostic assays. The Senior Quality Associate will drive change control, investigation of non-conformances, CAPA management, and audit readiness, while collaborating closely with lab scientists and regulatory teams. The position plays a key role in enabling biomarker-driven clinical trials through robust, patient-ready diagnostic solutions.

AstraZeneca Cambridge, United Kingdom

Senior Mechanical Engineer

Design and develop advanced electro-mechanical systems for medical technology applications, from concept through to manufacture. Work within a multidisciplinary team to solve complex engineering challenges and ensure compliance with regulatory standards. Contribute to innovative products that have a real-world impact on healthcare.

AES Ely, Cambridgeshire, United Kingdom £50,000 – £75,000 pa

Hybrid Permanent

Biomedical Scientist

This role involves performing routine and specialist clinical chemistry testing, operating and maintaining Beckman Coulter analysers, and ensuring accurate result validation within a UKAS-accredited laboratory. The scientist will support daily lab operations, adhere to ISO 15189 standards, and use systems like WinPath LIMS and Remisol middleware. Emphasis is placed on quality control, compliance, and collaboration within a multidisciplinary clinical team.

Acorn by Synergie Uphill, Somerset, United Kingdom £25 ph

On-site Temporary

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

Test Engineer

This role involves designing and implementing quality test procedures for both software and hardware components of medical devices. Responsibilities include attending design meetings, writing test plans, analyzing opportunities for automated testing, and ensuring compliance with regulatory standards.

Quality Start Walsall, West Midlands (county), United Kingdom £30,000 – £35,000 pa

On-site Permanent

R&D Consultant - Drug Delivery Device Design - Cambridge

Lead the design and development of innovative drug delivery devices through early-stage concept creation, prototyping, and experimental design. Work within multidisciplinary teams to translate technical challenges into manufacturable medical solutions while advising clients on development pathways and regulatory considerations. Play a hands-on role in R&D leadership and technical mentorship.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom

On-site Permanent