Jobs in Exeter

Head of Precision Diagnostics External Engagement

This senior role involves leading business development and transactions in biomarker and diagnostics for GSK's Oncology division. Responsibilities include negotiating deals, aligning with R&D strategy, and collaborating with internal and external stakeholders to drive strategic alliances and complex collaborations.

GSK £242,250 pa

On-site Permanent

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMOs, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK Irvine, Alba / Scotland, KA12 8EL, United Kingdom

Hybrid Permanent

Senior Director, Search & Evaluation Late TA Lead, Immunology

This role involves leading strategic sourcing and evaluation of late-stage external Hematology therapeutic assets, engaging with key opinion leaders, and integrating innovation into portfolio planning. The position requires deep clinical expertise, a proven track record in deal-making, and strong collaboration with cross-functional teams.

CSL £263,000 – £328,000 pa

Hybrid Permanent

Global Safety Lead - Formulation Safety

Located within CSLB’s GSPV department, the Director, Global Safety Lead, Formulation Safety provide expertise on all aspects of –clinical safety throughout the entire lifecycle of a product with special emphasis on ongoing evaluation of safety information during clinical development and...

CSL

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and ensuring data integrity for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also involves collaborating with various stakeholders, including external committees and site-facing colleagues, to ensure the successful execution of clinical studies.

Pfizer

On-site Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and ensuring data integrity for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also involves supporting site selection, protocol training, and continuous improvement initiatives to enhance clinical trial execution.

Pfizer

On-site Permanent

Senior Process Engineer

The Senior Process Engineer role at AstraZeneca involves developing and scaling up sustainable drug substance manufacturing processes. Responsibilities include introducing new equipment, optimizing processes, and collaborating with cross-functional teams to ensure robust and efficient production for clinical and preclinical trials.

AstraZeneca Macclesfield, United Kingdom

On-site Permanent

Senior Scientist, Translational PKPD

As a Senior Scientist in Translational PKPD Modeling & DMPK, you will apply your expertise in PKPD modeling and simulation to advance cancer biology understanding and accelerate drug discovery. You will provide specialist modeling input into pre-clinical projects, develop PKPD models, predict human dosing, and contribute to early clinical trials. This role involves cross-functional collaboration, strategic decision-making, and enhancing AstraZeneca’s translational research through publications and presentations.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Senior Systems Engineer, GXP Systems

The Role:Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.Moderna is establishing a leading research, development, and manufacturing facility at...

Moderna

On-site Permanent

Senior Computational Biologist, Tooling

In this role, you will work on the Value Tech Tooling Team at the forefront of drug discovery, using massive data capabilities to develop and maintain robust data pipelines and analytical workflows. You will collaborate with a cross-functional team of computational biologists, engineers, and scientists to turn complex analyses into reusable tools and pipelines, accelerating the discovery of life-changing therapeutics.

Recursion London, United Kingdom

On-site Permanent

Principal Scientist, TechBio Discovery

Your work will change lives. Including your own.The Impact You'll MakeRecursion is at the forefront of reimagining drug discovery by integrating technological innovations across biology, chemistry, automation, data science, and engineering to radically improve lives by industrializing drug discovery. We...

Recursion North Tyneside, NE29 8EP, United Kingdom US$198,000 – US$271,700 pa

Hybrid Permanent

Technical Program Coordinator, DDMR, London

As a Technical Program Coordinator, you will support the Drug Design and Medical Research (DDMR) function by managing program planning, monitoring timelines, tracking actions, and reporting risks. You will work closely with drug design teams, internal stakeholders, and external partners to ensure effective communication and alignment across the organization.

Isomorphic Labs London, United Kingdom

On-site Permanent

Senior Research Investigator, (Biologics Pharmacology), London

As a Senior Research Investigator, you will contribute to the pharmacology and translational biology strategy of novel large molecule therapeutics, leveraging Isomorphic Labs' cutting-edge AI drug design engine. You will design and execute pharmacology plans, lead in vivo and in vitro evaluations, and collaborate with interdisciplinary teams to advance drug discovery projects from early stages to clinical candidates.

Isomorphic Labs London, United Kingdom

On-site Permanent

Regulatory Transparency (Disclosures) Professional

In this role, you will manage the end-to-end execution of clinical trial registration and results posting, ensuring Roche complies with global regulations. You will lead the accurate and timely posting of clinical trial data, manage cross-functional teams, and ensure consistency and quality in all submissions.

Roche Welwyn Hatfield, United Kingdom

On-site Permanent

Lead Patent Paralegal

Work with usOur team are passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy and Autoimmune disease to deliver life-changing treatments to patients.Whilst working at Autolus you will enjoy a flexible, diverse and dynamic working...

Autolus London, W12 7RH, United Kingdom