Jobs in Reading

Commercial Head, Lung Europe

This role involves defining and leading the European commercial strategy for GSK’s lung oncology portfolio, ensuring alignment with global strategies and driving successful product launches across multiple European markets. Key responsibilities include performance management, cross-functional collaboration, and ensuring patient access to GSK medicines.

GSK

On-site Permanent

Senior Systems Engineer, GXP Systems

The Role:Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.Moderna is establishing a leading research, development, and manufacturing facility at...

Moderna Oxford, United Kingdom

On-site Permanent

Senior Systems Engineer, GXP Systems

The Role:Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.Moderna is establishing a leading research, development, and manufacturing facility at...

Moderna

On-site Permanent

Senior Clinical Trial Case Manager

This role involves leading cross-functional teams in reviewing safety data, mentoring junior staff, and ensuring compliance with GxP guidelines and international regulations. The position also focuses on managing pharmacovigilance procedures, conducting impact assessments of new legislation, and supporting regulatory inspections and audits.

CSL

On-site Permanent

PV Systems and Processes Lead x2

This role involves maintaining and improving CSL's global pharmacovigilance (PV) system, ensuring compliance with GVP and regulatory requirements. Responsibilities include leading investigations, managing deviations, coordinating inspections, and providing PV training across various functions and affiliates.

CSL United Kingdom

On-site Permanent

Regulatory Conformance Officer (12-month / Secondment)

As a Regulatory Conformance Officer, you will ensure that GSK's products meet all licensing and regulatory requirements, maintaining compliance with global market authorisations and supporting regulatory submissions. You will collaborate with multiple functions, including manufacturing, R&D, and global regulatory affairs, to deliver regulatory strategies and inspection readiness.

GSK Barnard Castle, United Kingdom

On-site Contract

Director, Process Engineering & Packaging

Leads process engineering and packaging for biologics at AstraZeneca, driving development of clinical and commercial drug product processes including fill/finish, device assembly, and packaging. Manages a team of scientists and engineers, oversees technology transfer across internal and external manufacturing sites, and advances design for manufacturability and regulatory strategies. Focuses on innovation, scale-up, and technical excellence within a global biopharmaceutical manufacturing network.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Senior Global Clinical Operations Director

This role leads the operational strategy and end-to-end delivery of global clinical programs in oncology, spanning early and late-phase development. The director will drive trial design, cross-functional collaboration, and regulatory readiness while managing complex multinational studies, CRO partnerships, and high-performing teams. Emphasis is placed on innovation, efficiency, and patient impact through advanced trial methodologies and strategic leadership.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Global Study Lead

The Global Study Lead is responsible for overseeing the design, planning, execution, and documentation of clinical studies, ensuring compliance with regulatory requirements and delivering high-quality results within budget and timelines. The role involves leading cross-functional teams, collaborating with internal and external stakeholders, and managing study-level budgets and operational aspects.

Roche

On-site Permanent

Associate Director, Statistical Programming

This role leads statistical programming efforts across global clinical trials, managing teams and driving innovation in data analysis and visualization. The individual will shape programming strategy, ensure audit readiness, and collaborate with cross-functional teams to deliver high-quality statistical outputs. Emphasis is placed on adopting modern tools like R, Shiny, and Git for reproducible, standardized workflows in drug development.

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

Hybrid Permanent

GCP Compliance Manager (GCO)

This role involves leading quality issue management, audit coordination, and inspection readiness for global clinical trials, ensuring compliance with GCP and regulatory standards. The manager will drive self-assessments, conduct risk-based investigations, and provide expert guidance across clinical operations. It’s a high-impact compliance position requiring strong cross-functional influence and operational rigor in a hybrid working environment.

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

Hybrid Permanent

VMG Access Technology & Operations Lead

This role involves leading the advancement of AI, digital tools, and operational capabilities across VMG Access at Pfizer. Key responsibilities include driving technology strategy, leading AI and automation initiatives, shaping GTCS-related technology changes, and enabling data-driven decision-making to support strategic and operational insights.

Pfizer London, SW7 2AP, United Kingdom

Hybrid Permanent

Head of Global Regulatory Affairs and Strategy

This senior leadership role involves defining and optimizing global regulatory strategies for drug development programs, building a regulatory team and systems, and implementing quality, pharmacovigilance, and medical writing frameworks. The role leverages AI to streamline regulatory workflows and ensure rapid global approval of products.

Isomorphic Labs Cambridge, United Kingdom

On-site Permanent

Head of Product Development & Engineering

This role involves leading the product development and engineering lifecycle for complex medical technology products, from concept to launch and ongoing support. Responsibilities include managing R&D projects, mentoring a specialist team, and collaborating with quality, operations, and commercial teams to ensure regulatory compliance and commercial success.

Concept Technical Worthing, West Sussex, United Kingdom £70,000 – £80,000 pa

On-site Permanent

Director, Medical Insights

The Director, Medical Insights role involves shaping and implementing Medical Insights processes, collaborating with various stakeholders to generate actionable insights, and embedding these insights into medical decision-making. The role focuses on advanced analytics, AI, and emerging technologies to drive value and impact across Pfizer’s medical portfolio.

Pfizer Test Valley, SO51 6HA, United Kingdom

Remote Permanent