Latest Drug Discovery Jobs

Associate Principal Computational Biologist, Neuroscience

This role involves leading computational biology efforts to support preclinical drug programs in neuroscience, integrating multi-omics data to validate therapeutic targets and accelerate drug discovery. The candidate will collaborate with biologists, chemists, and data scientists to generate actionable insights from high-dimensional datasets and support clinical development planning. Emphasis is placed on data integration, hypothesis generation, and cross-functional decision-making to advance therapies at scale.

Recursion United Kingdom US$200,600 – US$253,100 pa

Hybrid Permanent

Staff Product Manager, Agentic Systems

As the Staff Product Manager for Agentic Systems, you will define the technical and scientific capabilities for autonomous science, bridging the gap between in silico models and physical automated labs. You will lead hypothesis-driven product development, prioritize high-impact capabilities, and collaborate with cross-functional teams to optimize the drug discovery pipeline.

Recursion United Kingdom

Hybrid Permanent

Clinical Program Manager, Cambridge, MA

The Clinical Program Manager will lead the transition of internal drug programs from pre-IND stages into clinical trial execution, coordinating cross-functional global teams and external vendors. This role involves managing timelines, budgets, risks, and stakeholder communication, while leveraging AI-driven insights to accelerate development. The position emphasizes integrated project planning and operational leadership to ensure efficient, high-probability clinical advancement.

Isomorphic Labs Cambridge, United Kingdom

Hybrid Permanent

Bioanalytical Lead, London

This role involves leading bioanalytical strategy for AI-designed therapeutics across small molecules, biologics, and ADCs, from discovery through preclinical development. The candidate will design and validate PK, PD, and immunogenicity assays, manage global CROs, and integrate wet-lab data back into AI models to improve predictive accuracy. They will also author regulatory submissions and ensure compliance with GLP and ICH guidelines while navigating complex international sample logistics.

Isomorphic Labs London, United Kingdom

Hybrid Permanent

Associate Director, Diagnostic Planning Lead - Oncology

This role leads diagnostic planning initiatives within GSK’s Oncology Translational Medicine team, coordinating cross-functional efforts across clinical development, regulatory, and external partners to advance diagnostic assets. The position ensures alignment of project timelines, manages risks, and supports regulatory submissions, leveraging expertise in biomarkers and in vitro diagnostics within an oncology context.

GSK United States US$151,500 – US$252,500 pa

Hybrid Permanent

Associate Director, Diagnostic Planning Lead - Oncology

This role leads diagnostic planning initiatives within GSK’s Oncology Translational Medicine team, coordinating cross-functional projects and external partnerships to advance biomarker and diagnostic development. The position ensures alignment across clinical, regulatory, and commercial stakeholders, manages timelines and budgets, and supports regulatory submissions. It requires expertise in diagnostics, project management, and oncology drug development.

GSK US$151,500 – US$252,500 pa

Hybrid Permanent

Director, HTA, Value & Evidence (HV&E), PCOA

Develops and executes patient-centered outcomes assessment (PCOA) strategies in clinical trials and observational studies to support regulatory approval, market access, and reimbursement. Leads cross-functional collaboration with R&D, CMO, RWE, and Commercial teams, ensuring alignment with global regulatory and HTA requirements. Provides technical leadership in clinical outcome assessment (COA) methodology, evidence generation, and stakeholder engagement across Pfizer’s innovative therapy portfolio.

Pfizer US$176,600 – US$294,300 pa

Hybrid Permanent

Director, HTA, Value & Evidence (HV&E), PCOA

Develops and executes patient-centered outcomes assessment (PCOA) strategies in clinical and observational studies to support drug registration, access, and reimbursement. Leads evidence generation research, collaborates with cross-functional teams, and ensures alignment with regulatory and HTA guidelines. Manages external partners and promotes PCOA methodologies across Pfizer.

Pfizer United States US$176,600 – US$294,300 pa

Hybrid Permanent

Executive Director, Strategy, Oncology R&D

This role involves owning and driving the global Oncology R&D strategy, setting priorities for the senior executive team, and transforming the approach to deliver impact for patients. You will craft integrated therapeutic area strategies, combining clinical, scientific, and commercial insights to shape portfolio choices and investment priorities.

AstraZeneca London, United Kingdom

On-site Permanent

Executive Director, Strategy, Oncology R&D

This role involves crafting and driving the global Oncology R&D strategy, integrating clinical, scientific, and commercial insights to shape portfolio priorities. You will advise senior leadership on complex strategic decisions, optimize investment, and collaborate across functions to deliver impactful patient outcomes.

AstraZeneca Canterbury, United Kingdom

On-site Permanent

Virtual Analytics Network (VAN) PhD Graduate Program

This PhD Graduate Program at Novartis involves 15 months of rotations across three key areas of the organization, focusing on clinical trials and statistical analysis. After the rotations, you will work as a Principal Biostatistician, leading statistical tasks and innovative trial designs, collaborating with multi-functional teams and external stakeholders.

Novartis Ardross, Alba / Scotland, IV17 0YF, United Kingdom

Hybrid Permanent

Assoc Director, Statistical Programming

The Associate Director, Statistical Programming, leads all statistical programming aspects for one or more drug development programs, ensuring cross-functional collaboration, resource allocation, and regulatory compliance. They coordinate activities, mentor programmers, and represent the team in audits and Health Authority meetings.

Novartis London, United Kingdom

Hybrid Permanent

Regulatory Transparency (Disclosures) Professional

In this role, you will manage the end-to-end execution of clinical trial registration and results posting, ensuring Roche complies with global regulations. You will lead the accurate and timely posting of clinical trial data, manage cross-functional teams, and ensure consistency and quality in all submissions.

Roche Welwyn Hatfield, United Kingdom

On-site Permanent

Senior Project Specialist, Clinical Supplies

This role involves managing clinical supply operations for Moderna’s mRNA-based therapies, ensuring investigational products are labeled, packaged, and distributed efficiently to clinical sites. The specialist will coordinate with vendors, CROs, and internal teams to maintain supply chain compliance and continuity, while supporting digital innovation and process improvements in clinical supply workflows.

Moderna Oxford, United Kingdom

Hybrid Permanent

Senior Data Strategy & Analytics Specialist

This role involves designing and executing data strategies that integrate clinical, operational, and real-world data to support drug development. The specialist will act as a subject matter expert in data curation and analytics, working closely with scientific teams to improve data accessibility and usability. The position emphasizes the application of FAIR data principles and production-grade analytical workflows within a regulated environment.

Roche Welwyn Hatfield, United Kingdom

Hybrid Permanent