Latest Project Services Jobs

Quality Technology & Facilities Specialist

This role involves ensuring the compliance, quality, and operational effectiveness of technology systems and facilities across engineering, logistics, and new product introduction at GSK’s Barnard Castle site. The specialist will support validation, maintenance, change control, and continuous improvement initiatives, providing quality oversight and driving audit readiness. The position offers broad exposure to smart manufacturing technologies and cross-functional collaboration in a regulated environment.

GSK Barnard Castle, United Kingdom

On-site Permanent

Supported Studies Asset Study Delivery Lead - 14 month secondment

Leads end-to-end delivery of clinical study portfolios for a specific asset, coordinating proposal reviews for investigator-initiated and collaborative studies. Manages milestone tracking, budget forecasting, supply coordination, and stakeholder communication across cross-functional teams. Acts as primary operational contact and provides oversight in compliance with GCP and regulatory standards, while supporting team development and process improvements.

GSK United Kingdom

Contract

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12 Month University Industrial Placement Student (UIPS): Digital Health Strategy

This role involves supporting the development of digital health and AI strategies within Evinova, AstraZeneca’s health-tech subsidiary. You'll contribute to real-world initiatives in clinical development, conduct market and solution landscape research, track AI trends, and collaborate across teams to improve digital health solutions for patients and healthcare professionals.

AstraZeneca Cambridge, United Kingdom £28,000 pa

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12 Month University Industrial Placement Student (UIPS): Analytical Chemistry

This role involves supporting the development of pharmaceutical drugs through analytical chemistry techniques such as HPLC, GC, NMR, and mass spectrometry. You'll work within a dynamic team to ensure analytical data meets project timelines while adhering to GMP and GLP standards. The placement offers hands-on experience in a regulated lab environment and opportunities to present findings and develop scientific communication skills.

AstraZeneca Macclesfield, United Kingdom £28,000 pa

General Application - Register Your Interest

This is a general interest application for roles at Isomorphic Labs, an AI-driven drug discovery company. Candidates may be considered for positions including Software Engineers, ML Researchers, Computational Chemists, and Technical Project Managers. The role involves interdisciplinary collaboration to advance AI models for rational drug design and digital biology, within a culture emphasising curiosity, bravery, determination, and teamwork.

Isomorphic Labs United Kingdom

Hybrid Permanent

Study Grants Manager

The Study Grants Manager translates clinical trial protocols into accurate grant plans and fair market value assessments, supporting efficient site activation and budget forecasting. This role involves close collaboration with global study teams, country organizations, and vendors to optimize cost models and operational efficiency across clinical trials. It requires strong analytical skills, expertise in clinical development processes, and advanced use of tools like GrantPlan and MS Excel.

Novartis London, United Kingdom £49,140 – £91,260 pa

Hybrid Permanent

Scientific Engagement & Program Manager

This role involves planning and executing scientific engagement activities such as advisory boards, congress events, and medical education programs across key therapeutic areas including Oncology and Immunology. The individual will coordinate operational delivery, ensure compliance with SOPs, manage cross-functional collaboration, and support continuous process improvement within the IMACE Scientific Operations team. The position emphasizes project management, vendor coordination, and maintaining audit-ready documentation for medical and scientific initiatives.

Novartis London, United Kingdom £32,690 – £60,710 pa

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, resolves protocol issues, and supports enrollment and database release. The position requires extensive knowledge of GCP, regulatory standards, and therapeutic areas such as oncology, with frequent travel expected.

Pfizer United Kingdom

Remote Permanent

Clinical Research Associate

This role involves managing and monitoring clinical trial sites to ensure compliance with Good Clinical Practice, patient safety, and Pfizer's standards. The Clinical Research Associate serves as the primary point of contact for investigator sites, conducts remote and on-site monitoring, supports patient recruitment, and resolves protocol and data issues throughout the trial lifecycle. The position requires close collaboration with study teams and site personnel, with significant travel expected across the UK and internationally.

Pfizer United Kingdom

Remote Permanent

Bioinformatician - Pathogen

This role involves developing and refining bioinformatics workflows to analyse whole genome and metagenomic sequencing data for infectious disease diagnostics. The bioinformatician will work closely with wet lab scientists to interpret complex datasets, focusing on taxonomic classification, antimicrobial resistance prediction, and strain characterisation. The position supports a translational research initiative aiming to deploy scalable diagnostic tools globally.

Ellison Institute of Technology Oxford, United Kingdom

Hybrid Permanent

Fluidic System Engineer - Pathogen

Design and develop microfluidic systems for a point-of-care diagnostic device that enables metagenomic sequencing through a cartridge-based interface. Work closely with cross-functional teams to integrate microfluidics with instrumentation, electronics, and firmware, focusing on robustness, automation compatibility, and real-world performance. Conduct prototyping, testing, and validation using techniques like soft lithography and rapid prototyping to advance decentralized infectious disease diagnostics.

Ellison Institute of Technology Oxford, United Kingdom

On-site

Head of Computer-Aided Drug Discovery (CADD)

Lead a computational drug discovery team focused on structure- and fragment-based design, integrating AI/ML, cheminformatics, and advanced simulation methods into multidisciplinary drug discovery programmes. Drive computational strategy while maintaining hands-on involvement in projects from hit identification through to candidate nomination. Collaborate closely with medicinal chemistry, structural biology, and biophysics teams to deliver innovative therapeutics.

VRS UK Cambridge, Cambridgeshire, United Kingdom

Regional Operations Manager - Engineering

Oversee regional operations for engineering projects, ensuring on-time, on-budget delivery while managing multidisciplinary teams and cross-functional collaboration. Drive operational excellence through KPI monitoring, risk mitigation, and continuous improvement initiatives. Support commercial growth by aligning technical capabilities with strategic customer needs and contributing to innovation across global teams.

Averna Powered By Spherea East Parley, Dorset, United Kingdom

Senior Scientist (In vitro / Cellular Pharmacology), Cambridge, MA

This role involves designing and executing biological screening cascades to validate computational predictions in drug discovery. The scientist will lead biophysical, biochemical, and cellular assay development, collaborate with CROs, and bridge AI-driven insights with experimental validation across oncology and immunology programs. Close collaboration with medicinal chemistry, structural biology, and machine learning teams ensures data informs rational drug design.

Isomorphic Labs England

Hybrid Permanent

Senior Engineer, CSV Validation

This role involves end-to-end ownership of computerised system validation (CSV) for GxP-regulated systems used in the manufacturing and testing of advanced CAR-T cell therapies. The engineer will author and execute validation documentation, ensure compliance with international regulations (e.g. FDA 21 CFR Part 11, EU GMP Annex 11), manage change controls and CAPAs, and support regulatory inspections. The position requires strong technical writing, cross-functional collaboration, and expertise in GAMP 5 and data integrity within a biopharmaceutical context.

Autolus Stevenage, United Kingdom