Latest Project Services Jobs

NPI Quality Engineer

This role involves leading quality assurance throughout the new product introduction (NPI) process in a high-tech manufacturing environment. The engineer will ensure compliance with quality standards across design, development, and production, working closely with engineering, R&D, and supply chain teams. Key responsibilities include managing APQP/PPAP deliverables, leading root cause investigations, and driving continuous improvement in quality processes.

Yolk Recruitment Briton Ferry, West Glamorgan, SA11 2NH, United Kingdom £45,000 pa

On-site Permanent

Director, Clinical Trial and Data Transparency

This role involves providing strategic and operational expertise for the disclosure of clinical regulatory documents on public websites, ensuring compliance with global regulatory requirements. Responsibilities include managing disclosure activities, overseeing vendors, and developing standard processes and technologic solutions to support transparency in clinical trials.

Pfizer India

Remote Permanent

Director, Clinical Trial and Data Transparency

This role involves leading the strategic and operational aspects of clinical trial transparency and disclosure, ensuring compliance with global regulatory requirements. Responsibilities include managing disclosure activities, overseeing vendors, and developing standard processes for compliance.

Pfizer

Remote Permanent

Senior Clinical Development Medical Director

Salary Range:£96,036.50 - £178,353.50Job Description Summary#LI-HybridWork Arrangement: Hybrid WorkingLocation: London (The Westworks), United KingdomAre you passionate about shaping the future of clinical development and making a meaningful impact in Cardiovascular/Stroke medicine? We are looking for an experienced and visionary Senior...

Novartis

Global Development Lead, Early Clinical Development, Internal Medicine

The Global Development Lead will drive clinical research for cardiometabolic diseases, creating early clinical development strategies and leading the execution of research projects. They will translate pre-clinical observations into clinical experiments, manage clinical trial data, and collaborate with cross-functional teams to ensure medical and scientific excellence.

Pfizer United Kingdom

On-site Permanent

Global Development Lead, Early Clinical Development, Internal Medicine

The Global Development Lead will drive clinical research for cardiometabolic diseases, creating and executing early clinical development strategies. They will work closely with cross-functional teams to translate pre-clinical observations into clinical experiments, ensuring medical and scientific excellence in Phase 1/2 studies and regulatory submissions.

Pfizer London, SW7 2AP, United Kingdom

Hybrid Permanent

Senior Clinical Research Associate I

This role involves managing and monitoring clinical trial sites to ensure compliance with protocols, patient safety, and data quality. The Senior Clinical Research Associate I serves as the primary point of contact for investigator sites, conducts on-site and remote monitoring, supports enrollment, resolves protocol issues, and ensures adherence to Good Clinical Practice and regulatory standards. The position requires close collaboration with study teams and site staff within a flexible, remote-working environment.

Pfizer United Kingdom

Remote Permanent

Clinical Research Associate

This role involves managing and monitoring clinical trial sites remotely, ensuring compliance with Good Clinical Practice and Pfizer standards. The Clinical Research Associate serves as the primary point of contact for investigator sites, conducting remote and on-site monitoring, supporting patient safety, resolving protocol issues, and driving site activation and recruitment. The position emphasizes strong collaboration with study teams and site staff to maintain data quality and regulatory compliance throughout the trial lifecycle.

Pfizer United Kingdom

Remote Permanent

Senior Clinical Research Associate II

This role involves managing and monitoring clinical trial sites to ensure compliance with Good Clinical Practice and Pfizer standards, with a focus on patient safety and data quality. The Senior Clinical Research Associate acts as the primary point of contact for investigator sites, supporting study setup, execution, and closeout while addressing protocol issues and driving recruitment. The position requires extensive interaction with site staff, cross-functional teams, and vendors, using both on-site and remote monitoring methods.

Pfizer United Kingdom

Remote Permanent

VMG Access Technology & Operations Lead

This role involves leading the advancement of AI, digital tools, and operational capabilities across VMG Access at Pfizer. Responsibilities include driving technology strategy, implementing AI and automation, shaping GTCS-related changes, enabling data-driven decision-making, and ensuring compliance and risk management.

Pfizer Spain

On-site Permanent Flexible

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

Manufacturing Engineer

Manufacturing Engineer | Sheffield | £40,000-£50,000 + BenefitsW Talent is delighted to be partnering with a leading advanced manufacturing business in Sheffield to recruit a Manufacturing Engineer.This is an exciting opportunity to join a highly respected engineering organisation where you'll...

W Talent Sheffield, South Yorkshire, United Kingdom £40,000 – £50,000 pa

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

Global Labelling Associate Director, Content (Established Products)

This role involves developing and maintaining global labelling strategies and core documents for pharmaceutical products. You will lead cross-functional discussions, present labelling proposals, and ensure compliance with regulatory requirements across different markets.

Novartis

Hybrid Permanent

Global Program Safety Team Lead

This role involves leading the Medical Safety organization for Novartis' Neuroscience division, managing safety strategies, and influencing high-stakes decisions. Responsibilities include managing disease areas, enhancing team expertise, and ensuring robust safety evaluations throughout the product lifecycle.

Novartis United Kingdom

Hybrid Permanent