Latest Project Services Jobs

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK

Hybrid Permanent

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK

Hybrid Permanent

Vice President, Build — Data, Engineering & AI

Role purposeThe VP, Build — Data, Engineering & AI is the owner of the International Commercial build engine, accountable for turning prioritized demand into trusted, reusable and production-grade data, AI agents, solutions and technical services. The role owns the International...

Pfizer

Vice President, Build — Data, Engineering & AI

Role purposeThe VP, Build — Data, Engineering & AI is the owner of the International Commercial build engine, accountable for turning prioritized demand into trusted, reusable and production-grade data, AI agents, solutions and technical services. The role owns the International...

Pfizer

Support Engineer, London

As a Support Engineer, you will provide technical support, troubleshoot complex issues, and develop automation tools to improve efficiency. You will collaborate with other teams to resolve technical issues, manage 3rd party integrations, and contribute to the onboarding of new employees. This role is crucial for shaping the support strategy and driving innovation through automation.

Isomorphic Labs United Kingdom

Hybrid Permanent

Trial Vendor Senior Manager

This role involves managing all vendor-related aspects of global clinical trials, ensuring study outcomes are delivered on schedule, within budget, and to quality standards. You will collaborate closely with the Clinical Trial Team and vendor start-up managers, overseeing vendor interfaces, cost control, and service excellence.

Novartis United Kingdom

Hybrid Permanent Flexible

Medical Information Specialist

This role involves providing high-quality medical information to healthcare professionals, developing digital content for HCP and patient websites, and generating insights to support brand strategies. You will work closely with cross-functional teams to ensure clear and compliant scientific communication, focusing on Respiratory, Immunology, and Vaccines.

AstraZeneca London, United Kingdom

On-site Permanent

Quality Control Inspector

Quality Control InspectorBeckenham£32'000- £40'000 + Variety Of Work + Technical Training + Flexi Time + Competitive Pension + Stability + Family Feel Environment + Immediate StartAn excellent opportunity for a Quality Control Inspector with CMM inspection experience to join a...

Future Engineering Recruitment Ltd Beckenham, London, BR3 1DZ, United Kingdom £32,000 – £40,000 pa

Vendor Start-Up Manager - eCOA & Translations

The Vendor Start-Up Manager for eCOA and Translations ensures vendors are aligned and ready to deliver high-quality services from protocol finalization to database go-live. Key responsibilities include reviewing vendor specifications, coordinating kick-off meetings, performing User Acceptance Testing, and optimizing the study start-up process.

Novartis London, United Kingdom

Hybrid Permanent

Software Engineer

This role involves leading the development of Owkin’s Data Transformation Agent (DTA) and contributing to the core components of the platform. You will design and maintain complex data transformation workflows, manage deployments, and collaborate with internal stakeholders to ensure high standards in code and technical practices.

Owkin United Kingdom

Remote Permanent

Digital Health Connectivity Specialist

A global healthcare leader is expanding its UK connectivity team and has three exciting opportunities for experienced Healthcare IT professionals looking to develop their careers within an innovative, international organisation.This is a customer-facing role supporting the successful implementation and integration...

KirkhamYoung Ltd London, United Kingdom

Digital Health Connectivity Specialist

A global healthcare leader is expanding its UK connectivity team and has three exciting opportunities for experienced Healthcare IT professionals looking to develop their careers within an innovative, international organisation.This is a customer-facing role supporting the successful implementation and integration...

KirkhamYoung Ltd Bristol, Bristol (county), United Kingdom

Head of Medical & Scientific Affairs - Respiratory & Immunology

This role involves leading the national medical strategy for respiratory and immunology therapies within the UK NHS landscape, focusing on transforming patient care pathways and accelerating access to innovative treatments. The individual will drive pre-launch and launch readiness initiatives, shape real-world evidence generation, and collaborate with cross-functional teams and external stakeholders including NICE and MHRA. Leadership of field medical teams and strategic input into regulatory, market access, and digital health initiatives are central to the position.

AstraZeneca London, United Kingdom

Hybrid Permanent

Global Study Lead

The Global Study Lead is responsible for managing the full lifecycle of clinical studies, from design and planning to execution and documentation. Key responsibilities include leading the study team, ensuring compliance with regulations, managing budgets, and collaborating with cross-functional teams and external partners to deliver high-quality study results.

Roche United States US$100,400 – US$186,400 pa

On-site 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 US$100,400 – US$186,400 pa

On-site Permanent