Jobs in Exeter

Senior Director, Search & Evaluation Late TA Lead, Immunology

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.

CSL US$263,000 – US$328,000 pa

Hybrid Permanent

Director, Regional Ecosystem Lead (Northern Europe & UK)

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.

CSL United Kingdom

Hybrid Permanent

Field Service Engineer, Medical Diagnostic Systems

Perform on-site installation, maintenance, and repair of advanced medical diagnostic systems in NHS and private laboratories. Provide technical support and troubleshooting for complex laboratory equipment, working closely with lab managers and technicians. The role involves regular weekend work and extensive customer interaction across a diverse range of clinical environments.

TRS Consulting Kirkcaldy, Fife, KY1 1JA, United Kingdom £52,000 pa

Field Service Engineer, Medical Diagnostic Systems

Provide on-site service and repair for advanced medical diagnostic systems in NHS and private laboratories, ensuring minimal downtime and optimal performance. Troubleshoot complex technical issues and deliver customer training, working across diverse clinical environments. Role involves frequent site visits and weekend work as part of a five-day, seven-day schedule.

TRS Consulting Edinburgh, Alba / Scotland, United Kingdom £52,000 pa

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

This role involves leading clinical development for Internal Medicine assets within Pfizer's Research & Development division, with a focus on obesity-related therapies. The Global Development Lead will design and oversee global clinical trials, create development plans, and ensure regulatory compliance across regions including China and Japan. The position requires cross-functional leadership, engagement with external stakeholders, and contribution to regulatory submissions and product labeling.

Pfizer England £214,900 – £358,100 pa

On-site Permanent

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

Leads clinical development for assigned assets in Internal Medicine, serving as the primary clinical accountability point within Pfizer's Research & Development. Designs and oversees global clinical trials, regulatory submissions, and cross-functional team coordination, with potential involvement in obesity-related late-stage programs. Engages with external stakeholders and ensures compliance with scientific, regulatory, and safety standards.

Pfizer England

On-site Permanent

SERM Scientific Director

This role involves leading pharmacovigilance and risk management strategies for GSK's global assets, with a focus on safety evaluation and benefit-risk management across clinical development and post-marketing settings. The position requires expert analysis of clinical and safety data, leadership in cross-functional governance teams, and strategic input into regulatory submissions and risk mitigation. It plays a critical part in ensuring patient safety and regulatory compliance within immunology and other therapeutic areas.

GSK United States US$169,950 – US$283,250 pa

On-site Permanent

SERM Scientific Director

This role involves leading pharmacovigilance and risk management strategies for GSK’s global assets, with a focus on immunology. The Scientific Director will evaluate safety data, lead cross-functional teams, and ensure compliance in clinical development and post-marketing settings. The position requires deep expertise in safety evaluation, signal detection, and international regulatory standards.

GSK US$169,950 – US$283,250 pa

On-site Permanent

Senior Scientist (In vitro / Cellular Pharmacology), Cambridge, MA

This role involves designing and executing biological screening cascades to validate computational predictions in drug discovery. The scientist will lead biophysical, biochemical, and cellular assay development, collaborate with CROs, and bridge AI-driven insights with experimental validation across oncology and immunology programs. Close collaboration with medicinal chemistry, structural biology, and machine learning teams ensures data informs rational drug design.

Isomorphic Labs England

Hybrid Permanent

Senior Scientist (In vivo Pharmacology & Translational Sciences), Cambridge, MA

Lead translational strategies for oncology and immunology programs by designing in vivo pharmacology and PK/PD studies to validate AI-designed drug candidates. Bridge computational predictions with experimental validation through CRO partnerships and biomarker-driven approaches. Drive preclinical data generation to inform clinical trial design and regulatory filings.

Isomorphic Labs England

Hybrid Permanent

Study Start-Up Lead (SSUL)

The Study Start-Up Lead (SSUL) drives efficient clinical trial start-up processes, ensuring timely site activation and regulatory compliance. Key responsibilities include strategic planning, operational oversight, and collaboration with external stakeholders to innovate and improve trial delivery.

Roche Welwyn Hatfield, United Kingdom

Country Study Start-Up Team Leader (cSTL)

Leads and optimises clinical trial start-up operations in the UK for Roche, ensuring regulatory compliance and efficient site activation. Oversees regulatory submissions, contract and budget strategy, and cross-functional collaboration with global teams. Champions innovation, process standardisation, and inclusive leadership within a matrixed environment.

Roche Welwyn Hatfield, United Kingdom

Analyst, Quality Control, Microbiology

This role involves performing routine environmental monitoring, water sampling, and microbiological testing (including sterility, bioburden, and endotoxin) for mRNA products in a GMP-regulated manufacturing environment. The analyst will support method transfers, data review, investigations, and compliance activities while working closely with internal teams and contract laboratories. Emphasis is placed on digital workflows, data integrity, and adherence to cGMP standards.

Moderna Oxford, United Kingdom

Senior Research Associate, Bioanalytical & Molecular Assays

This role involves developing, qualifying, and validating molecular bioanalytical assays—such as qPCR, ddPCR, and RT-qPCR—to support clinical pharmacokinetic and pharmacodynamic studies within a GCLp-compliant environment. The scientist will work closely with cross-functional teams to ensure robust data generation, maintain regulatory compliance, and integrate emerging digital and automation technologies into workflows. A strong focus on reagent management, assay documentation, and continuous process improvement is central to the position.

Moderna Oxford, United Kingdom

Hybrid Permanent

Executive Director, Asset Team Lead

The Executive Director, Asset Strategy Leadership, 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 strategic clarity and urgency in drug development, translating scientific complexity into actionable strategies.

Recursion United Kingdom