Jobs in London

Data Management Specialist, London

As a Data Management Specialist, you will work closely with discovery project teams to integrate and curate high-quality experimental data, supporting the development of groundbreaking AI/ML models for drug discovery. Your role involves collaborating with internal and external teams to ensure data integrity and efficiency, contributing to the broader data team's efforts to build a robust data asset.

Isomorphic Labs London, United Kingdom

On-site Permanent

Data Curator, London

As a Data Curator at Isomorphic Labs, you will work closely with AI experts and drug discovery scientists to curate high-quality, ML-ready datasets. Your role involves integrating large-scale biomedical and biochemical data, enhancing data quality, and collaborating across teams to build and improve data assets that fuel the company's mission to accelerate drug discovery using AI.

Isomorphic Labs London, United Kingdom

On-site Permanent

Global Regulatory Affairs Operations Resource Planner

This role involves partnering with stakeholders to gather and validate submission planning information, ensuring efficient resource allocation for regulatory submissions. You will contribute to process improvements and deliver metrics to support leadership decisions.

Novartis London, United Kingdom

Hybrid Permanent

Senior Scientific Writer II

The Senior Scientific Writer II role involves developing high-quality medical and scientific communications for Novartis, including slide decks, congress materials, and advisory board content. The position requires strong collaboration with cross-functional teams to ensure content accuracy, consistency, and compliance with internal and external standards.

Novartis London, United Kingdom

Hybrid Permanent

Field Service Engineer

The Field Service Engineer will be responsible for servicing, maintaining, and troubleshooting electro-mechanical medical devices across East and North London. The role involves hands-on work in medical environments, providing customer service and ensuring equipment reliability.

Redshore London, United Kingdom £40,000 – £45,000 pa

On-site Permanent

Clinical Evaluation Specialist - Radiology

Clinical Evaluation Specialist - Radiology/ImagingA client of mine, a consultancy working with different software and medical devices, is looking for a Clinical Evaluation Specialist with Radiology Imaging expertise.Essential experience:2+ years of patient care experienceExpertise in radiology/imaging or similarClinical research backgroundOffered:Up...

Computer Futures London, United Kingdom £75,000 – £90,000 pa

Principal Clinical Project Manager

This role leads complex or pivotal clinical trials from conception to closeout, overseeing cross-functional teams and vendor partnerships. The Principal Clinical Project Manager ensures study delivery within quality, timeline, and budget targets, applying risk-based quality management and driving inspection readiness. They also mentor junior staff and contribute to process improvements within clinical operations.

Autolus London, W12 7RH, United Kingdom

Hybrid Permanent

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development will lead clinical research activities for GSK’s oncology portfolio, collaborating with various stakeholders to develop and execute phase 1-3 clinical trials. Key responsibilities include protocol development, medical monitoring, safety data review, and strategic partnerships with key external experts.

GSK Stevenage, United Kingdom

Hybrid Permanent

Medical Director - Oncology Clinical Development

The Medical Director will lead the development of oncology treatments, collaborating with a multidisciplinary team to design and execute clinical trials from early to late stages. Responsibilities include medical oversight, protocol development, safety monitoring, and strategic partnerships with key stakeholders.

GSK

Hybrid Permanent

Associate Principal AI & ML Engineer – Evinova

As an Associate Principal AI & ML Engineer at Evinova, you will develop and integrate advanced algorithms and generative AI systems to optimize clinical trial design and improve drug development processes. Your role involves working with multi-source data, building production systems, and collaborating with cross-functional teams to drive impactful solutions.

AstraZeneca London, United Kingdom

Hybrid Permanent

Associate Director, CMC Regulatory Affairs

This role involves leading the development and implementation of CMC regulatory strategies for small molecule drugs in global clinical trials. Responsibilities include managing CMC submissions, providing regulatory guidance, and supporting cross-functional teams in navigating international regulations.

Recursion London, W1C 2QP, United Kingdom £88,200 – £111,100 pa

Hybrid Permanent Flexible

Head of DMPK

The Head of DMPK will lead the strategic direction of drug metabolism and pharmacokinetics, ensuring robust scientific excellence and predictive modeling. Key responsibilities include defining DMPK strategies, collaborating with data science teams, and leading a high-performing team.

Recursion London, United Kingdom £166,500 – £208,100 pa

Hybrid Permanent

R&D Design Engineer

The R&D Design Engineer will focus on the design, prototyping, and development of medical devices, ensuring they meet regulatory requirements and are ready for market. Responsibilities include risk analysis, process development, and introducing new technologies and materials.

Real Limerick, Limerick County, Ireland £35 – £39 ph

On-site Contract

Vulnerability Analyst

This role involves assessing known software vulnerabilities in Windows-based applications used in regulated medical devices. Responsibilities include performing exploitability and risk analysis, evaluating third-party component risks, and producing clear security documentation. The position requires 2+ years of commercial experience in application security and a strong understanding of CVEs and secure software concepts.

Real Limerick, Limerick County, Ireland £47 ph

Hybrid Contract

Regulatory Affairs Specialist

The role involves providing technical regulatory support for the international distribution of diagnostic products, ensuring compliance with CE marking and global medical device regulations. Responsibilities include validating product claims, maintaining up-to-date documentation, and reviewing complaints for regulatory reportability. The position is based at the Innovation Centre in Bedford with hybrid working options.

Swiss Precision Diagnostics GmbH Cardington, Bedfordshire, United Kingdom £30,000 – £35,000 pa

Hybrid Contract