Jobs in London

Senior Research Investigator (In-vitro / Cellular Pharmacology), London

This role involves designing and implementing biological screening cascades for drug discovery programs, with a focus on in-vitro and cellular pharmacology. The candidate will work cross-functionally with AI and drug design teams to generate high-quality biological data, support decision-making, and advance projects from early discovery to clinical development. Emphasis is placed on mechanistic understanding of drug-target interactions in oncology, immunology, and partnered portfolios.

Isomorphic Labs London, United Kingdom

Hybrid Permanent

Reward and People Analytics Partner, London

This role focuses on ensuring data integrity and operational efficiency within People systems, with responsibilities spanning data management, tool administration, compensation cycle support, and reporting. The individual will leverage AI and automation to streamline workflows, deliver insights on reward metrics, and enhance how the People team operates at scale. It's a data-driven position that bridges technical analysis with human resources operations in a high-impact AI-driven research environment.

Isomorphic Labs London, United Kingdom

Hybrid Permanent

Associate Director, Statistical Programming

This role leads statistical programming efforts across global clinical trials, managing teams and driving innovation in data analysis and visualization. The individual will shape programming strategy, ensure audit readiness, and collaborate with cross-functional teams to deliver high-quality statistical outputs. Emphasis is placed on adopting modern tools like R, Shiny, and Git for reproducible, standardized workflows in drug development.

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

Hybrid Permanent

Data Management & Infrastruture Manager

The role involves ensuring data governance frameworks are consistently applied across data ingestion, transformation, and usage processes. It acts as a bridge between business and technical teams, focusing on data quality, compliance, lineage, and lifecycle management. The position emphasizes coordination, documentation, and continuous improvement of data standards and governance practices.

Novartis London, United Kingdom £47,740 – £88,660 pa

Hybrid 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 CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK

Hybrid 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 CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK

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 collaborating with cross-functional teams to ensure compliance with US, EU, and ROW regulations.

Recursion United Kingdom £176,400 – £228,250 pa

Hybrid Permanent Flexible

Head of DMPK

The Head of DMPK will lead the DMPK strategy, ensuring scientific excellence and robust human dose projections. You will collaborate with data science and ML teams to refine predictive ADME models, support external partnerships, and develop a high-performing team.

Recursion United Kingdom US$284,900 – US$400,950 pa

Hybrid Permanent

Director, Evidence Generation

This role involves leading the scientific oversight of global evidence generation studies, from Phase IIIb/IV trials to real-world evidence programmes. You will develop and implement integrated evidence strategies, influence product medical strategy, and engage with global stakeholders, including key opinion leaders and patient organisations.

Novartis London, United Kingdom

Hybrid Permanent

Global Regulatory Associate Director, Life Cycle Management

Manages regulatory maintenance for a high-complexity pharmaceutical portfolio, ensuring compliance and timely submissions to global health authorities. Develops strategic input on safety reports, variations, and renewals, while leading responses to regulatory queries and supporting cross-functional initiatives. Plays a key role in lifecycle management of innovative medicines, requiring strong scientific interpretation and stakeholder collaboration.

Novartis £67,900 – £126,100 pa

Hybrid Permanent

Global Program Safety Team Lead

This role involves leading the Medical Safety organization for Novartis' Neuroscience division, managing safety strategies, and influencing high-stakes decisions. Responsibilities include managing disease areas, enhancing team expertise, and ensuring robust safety evaluations throughout the product lifecycle.

Novartis United Kingdom

Hybrid Permanent

GCP Compliance Manager - Clinical Programs & Trials

This role involves providing expert Good Clinical Practice (GCP) compliance guidance to clinical trial teams, supporting decision-making on complex regulatory issues, and ensuring adherence to quality standards across global clinical programs. The manager will lead investigations into quality issues, drive inspection readiness, and translate regulatory requirements into practical actions. Collaboration with cross-functional stakeholders is central to strengthening compliance and fostering a culture of data integrity and accountability.

Novartis London, United Kingdom

Hybrid Permanent

GCP Compliance Manager - Clinical Programs & Trials

This role involves providing expert Good Clinical Practice (GCP) compliance guidance to clinical trial teams, supporting decision-making on complex regulatory issues, leading quality issue resolution, and ensuring inspection readiness across global clinical programs. The manager will translate regulatory requirements into actionable insights, conduct self-assessments, and drive continuous improvement in compliance. Embedded within cross-functional teams, the role emphasizes proactive risk mitigation, data integrity, and collaboration with Quality Assurance and Development functions.

Novartis Ardross, Alba / Scotland, IV17 0YF, United Kingdom

Hybrid Permanent

Head, Global Medical Affairs Oncology

This role involves leading the global medical affairs strategy for oncology, shaping early portfolio decisions, and ensuring evidence plans meet stakeholder needs. Responsibilities include developing medical plans, generating innovative evidence, and building partnerships with healthcare professionals and scientific leaders.

Novartis London, United Kingdom

Hybrid Permanent

Risk Surveillance Lead

The Risk Surveillance Lead drives the adoption of RBQM practices in clinical trials, overseeing risk assessment, documentation, and continuous improvement. They work closely with cross-functional teams to ensure quality risk management and compliance with regulatory standards.

Novartis London, United Kingdom

Hybrid Permanent