Latest Pharmaceutical Scientist Jobs

Study Manager

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

GSK Poland

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

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

The Global Development Lead (GDL) in Internal Medicine is responsible for leading the clinical development of assigned assets, collaborating with cross-functional teams to design and execute clinical trials, and ensuring regulatory compliance. The role involves creating clinical development plans, providing expert input on trial design and execution, and engaging with external stakeholders to drive strategic insights and support regulatory submissions.

Pfizer

On-site Permanent

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

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing, executing, and interpreting clinical studies, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally. The role also includes providing expert input on trial design, regulatory activities, and engaging with external stakeholders to drive strategic insights.

Pfizer US$214,900 – US$358,100 pa

On-site 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

Senior Clinical Trial Manager

Manages clinical trial operations from start-up to closure, coordinating with CROs and internal teams to ensure timely delivery of trials in oncology and rare diseases. Focuses on process improvements and operational excellence within a fast-paced, AI-driven drug discovery environment.

Recursion London, United Kingdom £62,400 – £84,000 pa

Hybrid Permanent

Automation/Process Control Engineer

This role involves strengthening control systems in AstraZeneca's manufacturing network, using digitalization and Lean techniques to improve production speed, resilience, and quality. The engineer will manage small projects, provide technical support, and mentor peers in automation and control systems.

AstraZeneca Macclesfield, United Kingdom

On-site Contract

Associate Director Clinical Supply IRT

This role involves leading the onboarding and continuous improvement of IRT standards and studies for AstraZeneca's clinical trials. Responsibilities include technical documentation, risk assessment, test script development, training, and process optimization. The position requires deep knowledge of R&D supply chain, clinical development processes, and IRT systems, with a focus on delivering high-quality, efficient clinical trial supplies.

AstraZeneca Macclesfield, United Kingdom

On-site Permanent

Global Clinical Operations Budget Manager

This role involves managing budgets and financial forecasts for clinical trials, working closely with clinical and finance teams to ensure accuracy and transparency. You will translate complex study assumptions into actionable financial insights, optimize trial delivery, and support process improvements in a global matrix environment.

Novartis London, United Kingdom

Hybrid Permanent

Global Regulatory Affairs Associate Director (Cardio-Metabolic)

This role involves leading the development and submission of regulatory documents, providing strategic direction, and negotiating with health authorities to expedite approvals. The position also focuses on ensuring compliance and timely approval of new and marketed products, serving as a regulatory liaison throughout the product lifecycle.

Novartis London, United Kingdom

Hybrid Permanent