Latest Project Services Jobs

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 London, United Kingdom

Hybrid Permanent

Associate Director, Global Publications & Foundational Content

Salary Range:£67,900.00 - £126,100.00Job Description SummaryAre you passionate about transforming complex scientific data into publications that shape healthcare and improve patient outcomes worldwide? As an Associate Director, Global Publications & Foundational Content, you will lead the development of high-impact scientific...

Novartis London, United Kingdom

Business Development Director

£75,000 - £80,000 per annum + 20% Bonus + Car AllowanceOffice is based in Hampshire, close to the Surrey borderFull Time | PermanentRegular UK Travel requiredOur client is an established international manufacturing and engineering business supplying innovative material solutions to...

HR Dept (Recruitment Agency) Farnborough, Hampshire, GU14 7JT, United Kingdom £75,000 – £80,000 pa

Product Manager

Product ManagerCambridgeUp to £70,000 + benefitsRole Overview: Product Manager:The company is looking for a technically competent Product Manager to lead global commercial and strategic activities for their range of scientific products used in the food & beverage markets. The role...

Marcus Webb Associates Limited Cambridge, Cambridgeshire, United Kingdom £60,000 – £70,000 pa

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

Clinical Research Scientist

This role involves the critical review and evaluation of clinical data from scientific literature and post-market sources, supporting regulatory compliance for medical devices. The Clinical Research Scientist will prepare technical and clinical evaluation reports aligned with MDR and IVDR standards, ensuring CE marking requirements are met. Emphasis is placed on scientific writing, data analysis, and cross-functional communication within a regulated manufacturing environment.

Randstad Delivery Witney, Oxfordshire, United Kingdom £32,500 pa

On-site Contract

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