Latest Drug Discovery Jobs

Senior Alliance Manager, London

This role involves managing strategic partnerships in a cutting-edge AI-driven drug discovery environment, ensuring scientific and commercial success. The Senior Alliance Manager will oversee alliance governance, drive collaboration frameworks, and support high-impact partnerships from research to development. A key focus is fostering strong relationships between internal teams and external partners while advancing best practices in alliance management.

Isomorphic Labs London, United Kingdom

Hybrid Permanent

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

Director, AI/ML MIDD Oncology Clinical Pharmacology, Modeling and Simulation

Lead and execute model-informed drug development strategies in oncology, applying advanced pharmacometric and AI/ML techniques to optimize clinical trial design, dose selection, and regulatory submissions. Drive innovation in quantitative clinical pharmacology across the R&D pipeline, from early development through lifecycle management, within a multidisciplinary translational medicine team.

GSK £119,250 – £198,750 pa

Director, AI/ML MIDD Oncology Clinical Pharmacology, Modeling and Simulation

Lead and deliver model-informed drug development (MIDD) strategies in oncology, applying advanced pharmacometric and AI/ML techniques to optimize clinical trial design, dose selection, and regulatory submissions. Work across multidisciplinary teams to advance GSK’s oncology pipeline using quantitative approaches including exposure-response modeling, disease progression models, and simulation-based trial design. Drive innovation through external collaborations, publications, and adoption of cutting-edge methodologies in clinical pharmacology.

GSK

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

Director, Clinical Pharmacology

Lead clinical pharmacology and pharmacometrics strategy across rare disease and oncology programs, designing studies and supporting regulatory submissions. Oversee modeling and simulation to inform dose selection and development decisions, working closely with cross-functional teams in a TechBio environment powered by AI-driven drug discovery. Serve as the primary expert in regulatory interactions related to clinical pharmacology.

Recursion London, United Kingdom £118,300 – £136,500 pa

Hybrid Permanent

Senior Director, Transactions - Oncology R&D

This role involves leading and executing strategic transactions in oncology R&D, including licensing, partnerships, and collaborations. The individual will structure deals, negotiate terms, and work cross-functionally to align external innovation with AstraZeneca’s oncology pipeline. It emphasizes leadership in deal execution and building scientific networks to advance cancer research.

AstraZeneca Cambridge, United Kingdom US$200,799 – US$301,199 pa

Senior Director, Transactions - Oncology R&D

This role leads the execution of business development transactions within AstraZeneca’s Oncology R&D, including licensing, partnerships, and collaborations. The individual will structure and negotiate deals, align them with strategic goals, and ensure smooth transition post-close. The position plays a central role in shaping the oncology innovation pipeline by leveraging external scientific and technological advancements.

AstraZeneca United States US$200,799 – US$301,199 pa

Senior Clinical Trial Case Manager

Manages clinical trial case management activities, ensuring compliance with international and national regulations including GxP and pharmacovigilance standards. Oversees safety reporting, vendor performance, and case processing for serious adverse events, while acting as a key liaison for inspections and audits. Provides training, supports database enhancements, and ensures accurate coding and consistency in safety data analysis.

CSL

Vaccines Safety Sciences Lead

Leads and manages pharmacovigilance safety sciences functions, ensuring compliance with global regulatory standards and overseeing signal detection, safety data analysis, and process optimization. Provides strategic direction for evolving PV legislation and acts as a subject matter expert in audits and inspections. Supports drug development and post-marketing safety reporting while driving data visualization and analytical improvements.

CSL

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

Software Manager

Lead a team of software and firmware engineers developing medical technology and connected devices in a regulated environment. Drive technical excellence across the full software development lifecycle, from architecture to validation, while fostering a culture of innovation and collaboration. Work closely with cross-functional teams to deliver integrated, safety-critical solutions.

SRG Sedgefield, County Durham, United Kingdom £55,000 – £65,000 pa

Senior Principal Statistical Programmer

Leads statistical programming for clinical studies across phases I-IV, ensuring high-quality, regulatory-compliant deliverables for regulatory submissions and clinical study reports. Develops and validates datasets and outputs using SAS, drives CDISC standards (SDTM/ADaM), and collaborates with biostatistics and cross-functional teams. Provides technical leadership, mentors junior programmers, and contributes to process improvements and programming specifications.

Novartis London, United Kingdom

On-site Permanent

Analyst, Quality Control, Microbiology

This role involves performing routine environmental monitoring, water sampling, and microbiological testing (including sterility, bioburden, and endotoxin) for mRNA products in a GMP-regulated manufacturing environment. The analyst will support method transfers, data review, investigations, and compliance activities while working closely with internal teams and contract laboratories. Emphasis is placed on digital workflows, data integrity, and adherence to cGMP standards.

Moderna Oxford, United Kingdom