Latest Drug Discovery Jobs

Manager, Computational Biology (Early Oncology)

Lead a team of computational biologists to integrate multi-omics data for oncology target discovery and validation, while actively contributing to analyses and mentoring team members. Drive biomarker strategy and patient stratification to advance precision oncology programs. Collaborate closely with biologists, chemists, and clinical teams to deliver data-driven insights that accelerate drug development.

Recursion United Kingdom US$151,800 – US$230,000 pa

Hybrid Permanent

Research Associate, Assay Operations (Contractor)

This role involves executing high-throughput, multi-omics screening experiments using automated lab systems in 384- and 1536-well plates to generate data for drug discovery. The candidate will prioritize production workflows, maintain equipment and reagents, and contribute to process improvements through automation and optimization. Collaboration, proactive communication, and adherence to SOPs are essential in this fast-paced, mission-driven environment.

Recursion United Kingdom

On-site Contract

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

Bioinformatics Engineer, London

This role involves building and maintaining a high-fidelity biological data layer to support machine learning at Isomorphic Labs. You will develop large-scale bioinformatics pipelines, harmonize public and internal datasets, and collaborate with cross-functional teams to ensure data quality and standardization. Your work will directly accelerate drug discovery by providing robust, integrated biological data for AI-driven research.

Isomorphic Labs London, United Kingdom

Hybrid Permanent

Executive Director, Oncology Search & Evaluation

This role involves leading oncology business development and licensing initiatives at GSK by identifying and evaluating external innovation opportunities. The Executive Director will lead due diligence, build strategic partnerships with biotech firms, and present investment recommendations to senior leadership. It requires deep scientific expertise, deal-making experience, and the ability to navigate complex cross-functional environments to advance GSK’s oncology pipeline.

GSK £229,350 – £382,250 pa

Hybrid Permanent

Senior Director, Translational Genetics

Leads a team of translational genetics scientists to drive data-driven insights in drug discovery and development, integrating genetic, genomic, and clinical data to address key translational questions across therapeutic areas. Focuses on target validation, biomarker discovery, and patient subgroup identification using advanced statistical genetics and analytical methods. Operates in a multidisciplinary environment, fostering innovation and external collaborations to accelerate the GSK pipeline.

GSK Stevenage, United Kingdom US$207,075 – US$345,125 pa

Hybrid Permanent

Quality Oversight and Compliance Director

The Quality Oversight and Compliance Director will lead the development and maintenance of Quality Plans, ensure inspection and audit readiness, and provide quality oversight of process deviations and investigations. This role involves interpreting and applying regulatory requirements, identifying and mitigating compliance gaps, and driving continuous improvement in pan-regulatory processes and data quality.

Pfizer London, SW7 2AP, United Kingdom

On-site Permanent

Senior Clinical Research Associate I

This role involves managing and monitoring clinical trial sites to ensure compliance with protocols, patient safety, and data quality. The Senior Clinical Research Associate I serves as the primary point of contact for investigator sites, conducts on-site and remote monitoring, supports enrollment, resolves protocol issues, and ensures adherence to Good Clinical Practice and regulatory standards. The position requires close collaboration with study teams and site staff within a flexible, remote-working environment.

Pfizer United Kingdom

Remote Permanent

Associate Director Clinical Supply IRT

This role involves leading the onboarding and continuous improvement of IRT standards and studies for AstraZeneca's clinical trials. Responsibilities include technical documentation, risk assessment, test script development, training, and process optimization. The position requires deep knowledge of R&D supply chain, clinical development processes, and IRT systems, with a focus on delivering high-quality, efficient clinical trial supplies.

AstraZeneca Macclesfield, United Kingdom

On-site Permanent

mRNA Senior Scientist

Job Title: mRNA Senior ScientistLocation: Cambridge, UKCompetitive Salary & Excellent Company Benefits!Diverse Minds, Bold Disruptors, Meaningful ImpactAstraZeneca is a global, innovation-driven BioPharmaceutical business that focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s most...

AstraZeneca Cambridge, United Kingdom

Associate Director, Regulatory Project Manager

Lead global regulatory project planning and execution across CSL’s product portfolio, ensuring timely submissions and alignment with strategic initiatives. Oversee cross-functional teams, drive process improvements, and ensure compliance with global health authority requirements. Mentor junior staff and contribute to governance and standardization in regulatory operations.

CSL US$170,000 – US$210,000 pa

Hybrid Permanent

Associate Director, Regulatory Project Manager

Leads global regulatory project planning and execution across CSL’s product portfolio, overseeing submission coordination and cross-functional collaboration to meet health authority requirements. Drives process improvements and operational excellence within regulatory operations, aligning initiatives with strategic priorities. Mentors junior staff and supports standardization of regulatory processes across regions.

CSL US$170,000 – US$210,000 pa

Hybrid Permanent

Business Development Consultant - Drug Delivery Devices

This role involves leading the development of next-generation drug delivery devices by managing multidisciplinary R&D teams and driving new business opportunities. The consultant will take ownership of programme management while remaining technically engaged in project delivery, supporting innovation in medical technology. A key aspect includes mentoring junior team members and contributing to high-impact, industry-disrupting solutions.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom

On-site Permanent

R&D Consultant - Drug Delivery Device Design - Cambridge

Lead the design and development of innovative drug delivery devices through early-stage concept creation, prototyping, and experimental design. Work within multidisciplinary teams to translate technical challenges into manufacturable medical solutions while advising clients on development pathways and regulatory considerations. Play a hands-on role in R&D leadership and technical mentorship.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom

On-site Permanent

(Fixed-Term) Manufacturing Associate, Drug Substance - Shift Position

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 Oxford, United Kingdom