Latest Drug Discovery Jobs

General Application - Register Your Interest

This is a general interest registration for roles at Isomorphic Labs, a company leveraging advanced AI to accelerate drug discovery and transform digital biology. The team seeks interdisciplinary experts in software engineering, machine learning, computational chemistry, and project management to contribute to groundbreaking scientific innovation. Work involves developing AI-driven models for rational drug design across multiple therapeutic areas.

Isomorphic Labs United Kingdom

Hybrid Permanent

Support Engineer, London

As a Support Engineer, you will provide technical support, troubleshoot complex issues, and develop automation tools to improve efficiency. You will collaborate with other teams to resolve technical issues, manage 3rd party integrations, and contribute to the onboarding of new employees. This role is crucial for shaping the support strategy and driving innovation through automation.

Isomorphic Labs United Kingdom

Hybrid Permanent

Director, Clinical Pharmacology

This role involves leading the clinical pharmacology and pharmacometrics strategy for rare disease and oncology programs. Responsibilities include designing clinical studies, authoring regulatory documents, and collaborating with cross-functional teams to expedite drug development.

Recursion North Tyneside, NE29 8EP, United Kingdom US$212,900 – US$297,000 pa

Hybrid Permanent

Interested in an ?

This role is not currently available, but the company is collecting resumes for future internships. Recursion is a clinical-stage TechBio company using AI and automation to advance drug discovery and development across various therapeutic areas.

Recursion United Kingdom

Remote Internship Part-time

AI Strategy Director, Development Operations

The AI Strategy Director role involves driving the AI-native Development Operations strategy at GSK, focusing on identifying and deploying AI solutions that create meaningful value in clinical trials. Responsibilities include prioritizing AI opportunities, evaluating vendor capabilities, and leading the deployment of AI-enabled workflows across the organization.

GSK

On-site Permanent

Manager, Translational Biomarker Data Pathways & Re-use

This role involves leading the setup, stabilization, and scaling of end-to-end translational data pathways at GSK. Key responsibilities include ensuring biomarker datasets are reusable, accessible, and aligned with translational decision-making, while also identifying and resolving systemic barriers and developing repeatable processes.

GSK

Hybrid Permanent

Process Engineer - Drug Substance Manufacture (DSM)

This role involves optimizing chemical manufacturing processes for drug substances in a regulated pharmaceutical environment. The engineer will lead process improvements, scale-up projects, and technology transfers while ensuring compliance with safety, quality, and environmental standards. Work includes root-cause analysis, change control management, and cross-functional collaboration to enhance capacity, robustness, and efficiency in API production.

AstraZeneca Macclesfield, United Kingdom

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

(Fixed Term) Analyst, Quality Control, Microbiology

The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology, with a diverse pipeline of development programs across various diseases.As an employee, you'll be part of a continually growing organization,...

Moderna Gargrave, BD23 3RZ, United Kingdom

Associate Director, Regulatory Diagnostics

Designs and leads global regulatory strategies for precision diagnostics, including companion diagnostics and in vitro devices, integrated within drug development programs. Works cross-functionally to manage submissions, health authority interactions, and compliance across lifecycle stages in a collaborative, innovation-driven environment.

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

Hybrid Permanent

Global Labelling Director, Content (Immunology)

The Global Labelling Director, Content (Immunology) will lead the development and delivery of high-quality global labelling strategies for innovative medicines. Key responsibilities include shaping labelling content, ensuring regulatory compliance, and collaborating with cross-functional teams to support successful product submissions and patient safety.

Novartis London, United Kingdom

Hybrid Permanent

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

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing, executing, and interpreting clinical studies, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally. The role also includes specialized monitoring, regulatory support, and engaging with external stakeholders to drive strategic insights.

Pfizer United States

On-site Permanent

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

The Global Development Lead (GDL) is responsible for leading the clinical development of internal medicine assets, working with cross-functional teams to design and execute clinical trials. Key responsibilities include creating clinical development plans, ensuring regulatory compliance, and collaborating with external partners to advance Pfizer's clinical programs.

Pfizer

On-site Permanent