Latest Drug Discovery Jobs

Research Engineer (LLM Performance), London

You will work on optimizing large language models for performance and scalability within a cutting-edge AI-driven drug discovery environment. The role involves implementing post-training methods, diagnosing distributed system bottlenecks, and deploying low-precision techniques to support real-world drug design applications. Collaboration with interdisciplinary research teams is central to translating novel AI methods into production-ready systems.

Isomorphic Labs London, United Kingdom

Senior Clinical Trial Manager, Cambridge, MA

The role involves end-to-end management of clinical trials within a fast-paced, AI-driven drug discovery environment. The Senior Clinical Trial Manager will lead cross-functional teams, oversee trial start-up through close-out, ensure compliance with ICH/GCP standards, and integrate AI innovations into clinical operations. Key responsibilities include vendor and budget management, clinical documentation, data oversight, and supporting regulatory readiness and audits.

Isomorphic Labs Cambridge, United Kingdom

Hybrid Permanent

Interested in an ?

This role involves joining Recursion's Internship Talent Network to be considered for future internship opportunities within a TechBio company focused on AI-driven drug discovery. Interns will engage with a platform that integrates biology, chemistry, and clinical development using proprietary AI models and large-scale automated laboratories. The position emphasizes innovation, cross-functional collaboration, and rapid learning in a mission-driven environment aimed at addressing significant unmet medical needs.

Recursion United Kingdom

Remote Internship Part-time

Don't see what you're looking for?

This is a general talent network sign-up opportunity rather than a specific job role. Candidates can submit their resume for future consideration at Recursion, a clinical-stage TechBio company using AI and automated biology to accelerate drug discovery. The company emphasizes bold, ethical innovation and cross-functional collaboration to address unmet medical needs.

Recursion United Kingdom

On-site Permanent

Executive Medical Director, Clinical Development Lead - Oncology GU

This role involves leading the clinical development of oncology treatments, specifically in genitourinary cancers. Responsibilities include defining clinical strategies, leading governance discussions, and representing the asset in external engagements. The role emphasizes data-driven decision-making and leveraging advanced analytics.

GSK

Executive Medical Director, Clinical Development Lead - Oncology GU

This role involves leading the clinical development of oncology treatments, specifically in genitourinary cancers. Responsibilities include defining clinical strategies, leading cross-functional teams, and engaging with health authorities and external partners. The position emphasizes leveraging advanced analytics and AI to drive decision-making and innovation in clinical development.

GSK

Principal Engineer, Drug Product

The Principal Engineer, Drug Product will lead the development of global engineering standards for drug product processes, including filling, inspection, packaging, and labeling. They will manage capital projects, ensure regulatory compliance, and drive innovation in manufacturing technologies across Moderna’s global network.

Moderna United States £142,500 – £256,500 pa

Principal Engineer, Drug Product

The Principal Engineer, Drug Product will lead the development of global engineering standards for sterile drug product processes, including filling, inspection, packaging, and labeling. They will manage capital projects, ensure regulatory compliance, and drive innovation in manufacturing technologies across Moderna’s global network.

Moderna

Associate Director, Regulatory Diagnostics

This role involves designing and delivering global regulatory strategies for precision diagnostics, including companion diagnostics and in vitro devices, within drug development programs. The individual will lead regulatory submissions across the lifecycle, engage with health authorities, and ensure compliance with global regulations. Collaboration with cross-functional teams and external partners is central to advancing regulatory plans for innovative diagnostics in a hybrid working environment.

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

Hybrid Permanent

GCP Compliance Director (Program & Study)

Lead a team of GCP Compliance Managers to ensure global clinical trials adhere to Good Clinical Practice and regulatory standards. Drive inspection readiness, audit oversight, and quality issue management across clinical development programs. Shape compliance strategy and foster a culture of quality and continuous improvement within a matrixed pharmaceutical environment.

Novartis London, United Kingdom £83,510 – £155,090 pa

Hybrid Permanent

Mechatronics Design Expert - Medical Technology

This role involves designing and developing novel mechatronic systems for medical devices and biotechnology applications, working closely with a multidisciplinary team to take ideas from concept to manufacture. Responsibilities include creating intricate mechanisms and overseeing the overall development of complex machines.

Newton Colmore Cambridge, United Kingdom

Senior Safety Scientist / Associate Director / Director

This role involves leading pharmacovigilance and safety science activities across Roche’s medicine portfolio, with responsibilities spanning signal detection, risk management, and safety reporting. The individual will contribute to clinical development strategies, oversee post-market safety assessments, and ensure compliance with global regulatory standards. Working within a hybrid model in Welwyn, the position requires strong scientific analysis, leadership, and cross-functional collaboration in a regulated environment.

Roche Welwyn Hatfield, United Kingdom

Executive Director / Vice President, Business Development

Lead business development strategy to identify and execute strategic partnerships, in- and out-licensing deals, co-developments, and M&A opportunities in oncology and autoimmune disease. Represent Autolus at high-level meetings, build relationships across biotech, pharma, and academia, and collaborate with cross-functional teams to align BD initiatives with corporate goals. Requires deep expertise in biopharma deal-making and strong scientific-business acumen.

Autolus