Latest Drug Discovery Jobs

Team / Research Leader (Translational Oncology), London

This role involves leading the development and execution of comprehensive translational strategies for Isomorphic Labs' oncology pipeline. You will collaborate with interdisciplinary teams, manage a group of biologists, and ensure the successful transition of AI-designed drugs from preclinical to clinical stages.

Isomorphic Labs United Kingdom

Hybrid Permanent

Staff Engineer, AI Security and Product Security

This role involves leading product and AI security strategy across web, mobile, API, cloud, and container environments with a strong shift-left approach. The engineer will secure AI/ML systems, including LLM integrations, agentic pipelines, and MLOps infrastructure, while defending against AI-specific threats like prompt injection and model extraction. They will also drive secure development practices, conduct threat modeling, and lead incident response in collaboration with cross-functional teams.

Recursion United Kingdom US$186,900 – US$220,400 pa

Hybrid Permanent

Vice President, Head of Clinical Operations

This role involves leading the clinical operations strategy and execution across Recursion’s full clinical portfolio, from early-stage studies to pivotal trials and submission support. The VP will build scalable operating models, manage global trials, and ensure operational excellence in a data-driven, patient-centered, and technology-enabled environment.

Recursion North Tyneside, NE29 8EP, United Kingdom

On-site Permanent

Executive Director, Respiratory

Leads translational biology strategy in respiratory research, integrating human-centric science to drive target validation and clinical translation across diseases like COPD, IPF, and pulmonary hypertension. Builds and leads a multidisciplinary team, leveraging internal and external capabilities to advance GSK's respiratory portfolio with a focus on mechanistic insight and biomarker integration.

GSK Stevenage, United Kingdom

Hybrid Permanent

ViiV Healthcare (GSK) Medical Director, ViiV R&D Physician Center of Excellence

This Medical Director role involves leading Phase 1-4 clinical trials, ensuring the successful planning, execution, and reporting of protocols for innovative HIV treatments. The role requires strong medical governance, safety expertise, and cross-functional collaboration with internal and external stakeholders to advance ViiV's mission of delivering long-acting HIV therapies.

GSK United States

On-site Permanent

Director, Clinical Intelligence & Evidence – Cardiovascular, Renal and Metabolism

Role: Director, Clinical Intelligence & Evidence – Cardiovascular, Renal and MetabolismLocation: Cambridge UKSalary: Competitive + Excellent BenefitsAt AstraZeneca make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our...

AstraZeneca Cambridge, United Kingdom

Associate Director, Safety Epidemiology – Global Patient Safety

This role involves leading the design, execution, and reporting of post-authorisation safety studies using real-world data. The candidate will collaborate with various teams to produce high-quality evidence for regulatory decisions and risk management, ensuring AstraZeneca's medicines are safe and effective.

AstraZeneca Chatham, ME4 4NP, United Kingdom

On-site Permanent

Portfolio Innovation Director - Global Clinical Operations

Leads innovation in global clinical operations by identifying and integrating AI-driven and technology-enabled solutions into clinical trials. Focuses on improving trial design, patient access, and operational efficiency while working across cross-functional teams to scale impactful innovations. Requires deep clinical and drug development expertise to evaluate and implement transformative solutions.

Novartis Ireland

Hybrid Permanent

Global Program Regulatory Manager - Neuroscience

This role involves driving regulatory strategy and execution for neuroscience products across global markets, with a focus on preparing and submitting clinical trial applications, managing health authority interactions, and ensuring compliance throughout the product lifecycle. The manager will work cross-functionally to translate scientific data into regulatory submissions and support timely approvals. It is a hybrid role based in London, requiring strong expertise in pharmaceutical regulatory affairs.

Novartis

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are on time, on budget, and compliant with standards. Key responsibilities include monitoring study conduct, drafting clinical documents, coordinating meetings, and managing study communications and budgets.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are on time, on budget, and compliant with standards. Responsibilities include monitoring study progress, drafting key documents, coordinating meetings, managing communications, and overseeing clinical supplies and budget tracking.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are delivered on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, managing study communications, and overseeing clinical supply and investigational product delivery.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are on time, on budget, and compliant with standards. Responsibilities include monitoring study progress, drafting key clinical documents, coordinating meetings, managing study communications, and overseeing clinical supply and investigational product delivery.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are delivered on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and budgets.

GSK

Hybrid Permanent

Clinical Sciences Manager, Global Collaborative Studies – ViiV Healthcare 10 month maternity cover

This role involves leading and managing ViiV Healthcare's supported studies, including investigator-sponsored and collaborative studies. Responsibilities include reviewing study proposals, ensuring compliance with policies, and maintaining strong relationships with external investigators and internal stakeholders.

GSK United Kingdom

On-site Temporary