Jobs in Exeter

Field Service Engineer, Medical Diagnostic Systems

This role involves servicing and repairing advanced medical diagnostic systems in NHS and private laboratory settings. The engineer will perform on-site maintenance, troubleshoot technical issues, and deliver customer support across pathology and clinical chemistry departments. Full product training is provided, and the role requires a flexible schedule including weekend work.

TRS Consulting Poole, Dorset, United Kingdom £52,000 pa

Field Service Engineer, Medical Diagnostic Systems

Provide on-site service and repair for advanced medical diagnostic systems used in NHS and private laboratories. Troubleshoot complex technical issues and deliver customer support to laboratory managers and technicians. Receive full product training and work across a range of high-value scientific equipment, with a focus on reliability and customer satisfaction.

TRS Consulting Bournemouth, Dorset, United Kingdom £52,000 pa

On-site Permanent

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

Leads clinical development for Internal Medicine assets within Pfizer's R&D organization, with end-to-end accountability for creating and executing global clinical development plans. Serves as the primary clinical point of contact across cross-functional teams and external partners, driving trial design, regulatory submissions, and lifecycle strategy. Focuses on obesity and related therapeutic areas, integrating innovation, patient engagement, and regulatory expertise to advance drug development.

Pfizer £214,900 – £358,100 pa

On-site Permanent

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

Leads clinical development for assigned internal medicine assets within Pfizer's Research & Development division, with end-to-end accountability for creating and executing global clinical development plans. Oversees cross-functional teams to design and deliver clinical trials supporting regulatory submissions, while providing therapeutic expertise in obesity and endocrinology. Engages external stakeholders and contributes to regulatory strategy, safety reporting, and product labeling.

Pfizer £214,900 – £358,100 pa

On-site Permanent

Maintenance Engineering Manager - Packaging

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.

Moderna

Hybrid Permanent

Sr. Manager, Site Budgets and Contracts

This role involves leading the creation and management of investigator site budgets and contracts for global clinical trials, using Grants Manager and FMV benchmarking tools. The Senior Manager collaborates with CROs, Legal, and Clinical Operations to ensure site budgets align with study forecasts and are executed on time. Responsibilities include strategic planning, contract negotiation oversight, risk identification, and process improvement within an outsourced trial model.

Moderna

Hybrid Permanent

Director, R&D AI & Technology Adoption

This role involves partnering with R&D technology programmes to create and deliver practical adoption plans for AI and digital tools. You will assess programme readiness, coordinate stakeholders, and measure the impact of new capabilities. The position requires strong project delivery and analytical skills, with a focus on driving organisational change and value creation.

GSK Stevenage, United Kingdom £170,775 – £284,625 pa

Medical Director-Oncology Clinical Development - GI

This role involves leading medical monitoring and safety oversight for gastrointestinal (GI) oncology clinical trials, contributing to study design, data interpretation, and regulatory interactions. The Medical Director integrates physician-level expertise into clinical development, working within cross-functional teams to ensure patient safety and scientific integrity. The position plays a key role in translating clinical data into actionable insights for advancing cancer treatments with high unmet need.

GSK Stevenage, United Kingdom US$222,750 – US$371,250 pa

Associate Director, Clinical Program Management, Cambridge, MA

The Clinical Program Manager will lead the transition of internal drug programs from pre-IND stages into clinical trial execution, coordinating cross-functional global teams and managing timelines, budgets, and vendor partnerships. The role leverages AI and emerging technologies to drive efficient clinical development with a focus on high-probability outcomes. It involves strategic oversight of CROs and collaborators while ensuring alignment between clinical objectives and company goals.

Isomorphic Labs England

Hybrid Permanent

Associate Director, Statistical Programming

Lead a global team of statistical programmers, driving standardization, innovation, and quality in clinical trial data analysis. Develop programming strategies using modern tools like R, Git, and AI-enabled technologies, ensuring audit-ready deliverables and alignment with biostatistics and data management. Provide technical leadership and influence global drug development strategy across phases I–IV studies.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

Translational Medicine Expert – Dermatology, Associate Director

This role involves providing medical and scientific leadership in translational medicine for dermatology programs, spanning early to late-stage drug development. The expert will design and implement strategies for clinical pharmacology, biomarker development, and regulatory submissions, while leading cross-functional teams and supporting in-licensing opportunities. Work includes oversight of clinical studies, publication strategy, and engagement with regulatory and external stakeholders.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

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

Senior Design Assurance Engineer

This role involves ensuring medical devices are developed in compliance with global regulatory standards, focusing on design control, risk management, and quality assurance throughout the product lifecycle. The engineer will support verification and validation activities, maintain Design History Files, and collaborate with cross-functional teams to drive compliance and continuous improvement. It's a key position within a regulated environment, emphasizing technical documentation, audit readiness, and adherence to ISO 13485 and ISO 14971.

SRG Cambridge, Cambridgeshire, United Kingdom £60,000 – £70,000 pa

Senior Scientist, AMR Genomics - Pathogen

This role involves curating expert rules for interpreting antimicrobial resistance (AMR) genotypic data, analysing whole genome sequences and antimicrobial susceptibility test (AST) results, and supporting the development of diagnostic tools. The scientist will investigate novel resistance mechanisms, collaborate on machine learning models, and contribute to a large-scale pathogen database using long-read sequencing. Work is primarily desk-based with opportunities for lab research and cross-team collaboration in a high-impact, translational environment.

Ellison Institute of Technology Oxford, United Kingdom

Hybrid Permanent

Director, Clinical Pharmacology

Lead clinical pharmacology and pharmacometrics strategy across rare disease and oncology programs, designing studies and supporting regulatory submissions. Oversee modeling and simulation to inform dose selection and development decisions, working closely with cross-functional teams in a TechBio environment powered by AI-driven drug discovery. Serve as the primary expert in regulatory interactions related to clinical pharmacology.

Recursion London, United Kingdom £118,300 – £136,500 pa

Hybrid Permanent