Latest Drug Discovery Jobs

Director of Nonclinical Safety, Cambridge, MA

Lead the development and execution of nonclinical safety strategies for small molecule drug candidates in oncology and non-oncology programs, integrating AI-driven predictive models with traditional toxicology. Build and scale the nonclinical safety function within an AI-first drug discovery environment, ensuring high-quality data feedback to refine computational models. Collaborate across preclinical, clinical, and regulatory teams to advance compounds through IND and NDA/MAA-enabling studies.

Isomorphic Labs Cambridge, United Kingdom

Security Engineering Manager, London or Lausanne

As a Security Engineering Manager, you will lead and scale a high-performing team responsible for securing Isomorphic Labs' AI-driven drug discovery platform. You'll define the technical security roadmap across cloud infrastructure, IAM, secure SDLC, and security monitoring, while enabling rapid innovation for ML researchers and drug discovery teams. The role involves pioneering AI-first security architectures, leading transformational projects, and acting as a key liaison within the Alphabet/Google ecosystem.

Isomorphic Labs United Kingdom

Medical Director Clinical Development- Aging

This role involves leading clinical development strategies for aging-related research within GSK’s Respiratory, Immunology & Inflammation unit. The Medical Director will design and deliver translational and clinical plans, oversee study execution, and provide scientific leadership across cross-functional teams. The position emphasizes innovation in immune science and data-driven decision-making to advance novel medicines through the pipeline.

GSK London, United Kingdom £189,750 – £316,250 pa

Medical Director Clinical Development- Respiratory

Leads clinical development for respiratory programs within GSK’s R&D pipeline, driving translational and clinical strategies from early to late stages. Provides medical oversight, designs studies, and collaborates across functions to deliver innovative medicines addressing immune-mediated respiratory diseases. Engages with regulators, investigators, and internal teams to advance asset development and shape future treatment paradigms.

GSK London, United Kingdom

Hybrid Permanent

Clinical Data Strategy, Manager

This role involves leading clinical data strategy planning and execution across Translational Medicine programs, with a focus on designing fit-for-purpose data collection approaches and supporting robust decision-making. The individual will develop Data Strategy Plans, guide trial teams on data oversight, and leverage internal and external data to inform trial design—particularly in Neuroscience. The position requires deep expertise in clinical assessments, data integrity, and cross-functional collaboration in a global, fast-paced environment.

Novartis London, United Kingdom £49,140 – £91,260 pa

Hybrid Permanent

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

This role leads clinical development for Internal Medicine assets within Pfizer's Research & Development division, serving as the primary clinical accountability point for global regulatory submissions. The individual will direct cross-functional teams in designing and executing Phase 1-3 trials, develop clinical development plans, and contribute to regulatory filings, safety reports, and product labeling. The position emphasizes leadership in obesity-related therapeutics, digital innovation in clinical development, and engagement with external scientific and regulatory stakeholders.

Pfizer

On-site Permanent

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

This role involves leading clinical development for Internal Medicine assets within Pfizer's Research & Development division, with a focus on obesity and chronic weight management. The Global Development Lead is responsible for end-to-end clinical strategy, including designing and executing global clinical trials, regulatory submissions, and cross-functional team leadership. The position requires deep therapeutic expertise, strategic input into product development, and engagement with external stakeholders such as advisory boards and regulatory bodies.

Pfizer US$214,900 – US$358,100 pa

On-site Permanent

(Fixed Term) Manufacturing Associate I

Operate production equipment for mRNA vaccine manufacturing in compliance with cGMP and safety standards. Perform routine maintenance, support deviation investigations, and contribute to continuous improvement in a highly regulated, technology-driven environment. Work collaboratively with QA and cross-functional teams to ensure timely batch disposition and operational excellence.

Moderna

On-site Temporary

(Fixed-Term) Manufacturing Associate I

Operate and maintain equipment in a cGMP-compliant, highly automated mRNA vaccine production environment at Moderna's Oxford facility. Perform production operations, support quality assurance, troubleshoot issues, and contribute to continuous improvement initiatives using digital systems and advanced manufacturing technologies. Work within a 2-2-3 rotating shift pattern to ensure reliable, safe, and compliant vaccine manufacturing.

Moderna Oxford, United Kingdom

Global Regulatory Associate Director, Life Cycle Management

Manages regulatory maintenance for a high-complexity pharmaceutical portfolio, ensuring compliance and timely submissions. Develops strategic regulatory input for safety reports, variations, and renewals, while acting as a liaison with health authorities. Supports global approval processes and contributes to process improvements and team mentorship.

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

Hybrid Permanent

Facilities Engineering Manager

This role involves providing technical leadership for facility and utility systems at Moderna’s biotech manufacturing site in Harwell. The Facilities Engineering Manager ensures operational reliability, oversees vendor performance, and drives maintenance excellence across R&D and manufacturing environments. The position emphasizes continuous improvement, compliance, and the use of digital tools including AI-enabled systems, within a GMP-regulated setting.

Moderna

On-site Permanent

(Fixed Term) Warehouse Specialist

This role involves managing warehouse operations within a 24/7 GMP environment to support mRNA vaccine manufacturing. The specialist ensures accurate receipt, storage, and distribution of materials, maintains inventory integrity via SAP, and complies with strict quality and safety standards. The position engages with digital systems and supports logistics across a highly regulated pharmaceutical setting.

Moderna Oxford, United Kingdom

On-site Permanent Shift-work