Latest Project Services Jobs

Senior Director / Director, Non-Clinical Safety Project Specialist

This role leads non-clinical safety strategy across drug discovery and development, integrating scientific data to inform project decisions, regulatory submissions, and risk assessment. The specialist provides expert guidance on safety profiling, candidate selection, and translational planning, while mentoring teams and shaping regulatory narratives. They work cross-functionally to ensure robust safety evaluation for small molecules and biologics through clinical and post-market stages.

GSK £224,400 – £374,000 pa

On-site Permanent

Senior Director / Director, Non-Clinical Safety Project Specialist

This role leads non-clinical safety strategy across drug discovery and development, integrating scientific data to inform project decisions, regulatory submissions, and risk assessment. The position involves mentoring teams, shaping translational plans, and providing expert input on safety profiling and candidate selection. It plays a key part in regulatory strategy and cross-functional leadership within a global biopharma environment.

GSK £224,400 – £374,000 pa

Hybrid Permanent

Senior Director Global Clinical Program Lead Cardiovascular & Renal

This role involves leading the clinical development and strategic oversight of a medicine for cardiovascular and renal conditions. Responsibilities include managing the Clinical Development Team, ensuring high clinical and scientific standards, and authoring key study documents and regulatory submissions.

CSL

On-site Permanent

Director, Regional Ecosystem Lead (Northern Europe & UK)

This role involves leading CSL's presence in key innovation hubs across Northern Europe and the UK, building strategic partnerships, and driving business development. The Director will maintain relationships with universities, incubators, and venture capital firms, and actively participate in industry events to enhance CSL's external brand and deal flow.

CSL

Hybrid Permanent

Research Synthesis Chemist

Your work will change lives. Including your own.The Impact You’ll MakeWe are growing our chemistry team at Recursion and are seeking a Research Synthetic Chemist to join our Automated Chemistry group. We are looking for an individual that thrives in...

Recursion Crathes, Alba / Scotland, United Kingdom

Global Labelling Associate Director, Content (Oncology)

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

Novartis

Hybrid Permanent

Global Labelling Associate Director, Content (Cardiovascular, Renal & Metabolism)

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

Novartis London, United Kingdom

Hybrid Permanent

Senior Automation Engineer - Pharmaceuticals

Lead the design and optimisation of automation systems within a pharmaceutical manufacturing environment, focusing on PLC, SCADA, HMI, and DCS platforms. Collaborate with cross-functional teams to support continuous improvement, capital projects, and system validation. Provide technical leadership and mentorship to junior engineers while ensuring high reliability and compliance in controlled processes.

Smart4Sciences North Yorkshire, United Kingdom

On-site Permanent

Embedded Systems Engineer

Embedded Systems EngineerA long-established global manufacturer of high-voltage power solutions used in medical devices, semiconductor equipment, scientific instruments and industrial systems. The organisation operates design and manufacturing facilities across North America, Europe and Asia and partners with leading OEMs developing...

Terry Parris Associates Codmore Hill, West Sussex, RH20 1DQ, United Kingdom

Graduate Quality Engineer

This role involves supporting quality management systems in a regulated pharmaceutical environment, with responsibilities including compliance monitoring, documentation review, and cross-functional collaboration during product development and manufacturing. The graduate engineer will apply risk management techniques, contribute to audits, and ensure procedural accuracy within a high-compliance setting. It offers early-career professionals hands-on experience in quality assurance within medical device production.

Randstad Delivery Witney, Oxfordshire, United Kingdom £33,000 – £45,000 pa

On-site Contract

Associate Director, Biostatistics 2

The role involves leading the statistical aspects of clinical development programs, including study design, data analysis, and regulatory submissions. Responsibilities include collaborating with cross-functional teams, managing CROs, and representing Biostatistics in regulatory interactions.

Appcast Enterprise Maidenhead, SL6 1QB, United Kingdom

On-site Permanent

Metabolite Identification Specialist

This role involves leading metabolite identification and biotransformation studies to determine the metabolic fate of drug candidates. The specialist will design and interpret advanced analytical data using techniques like high-resolution mass spectrometry, support drug discovery and development programmes, and provide scientific guidance to project teams and junior scientists. The position emphasizes technical leadership, problem-solving in complex metabolic pathways, and direct contribution to the progression of pharmaceutical candidates.

SRG Sandwich, United Kingdom

On-site Permanent

Senior Scientist or Associate Principal Scientist Metabolist Team

This role involves conducting advanced in vitro and ex vivo research to identify and validate therapeutic targets for obesity. The successful candidate will work in a dynamic, collaborative environment, designing and implementing experiments, analyzing data, and contributing to drug discovery projects across multiple sites.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Regulatory Affairs Assistant

The Regulatory Affairs Assistant will provide administrative, operational, and compliance support to the Regulatory Affairs team, ensuring accurate data and documentation, supporting team processes, and maintaining compliance with regulatory standards. The role involves a broad range of activities, including regulatory file compilation, database management, project coordination, and administrative support to the Head of Regulatory and the team.

AstraZeneca London, United Kingdom

On-site Permanent

Research Associate, Primary Pharmacology

This role involves developing and optimizing cell-based and biochemical assays to support small molecule drug discovery, with a focus on compound characterization and candidate identification. The scientist will work in a high-throughput, automated lab environment, generating decision-ready data in collaboration with cross-functional teams. The position emphasizes hands-on experimentation, assay innovation, and integration within a multidisciplinary drug discovery pipeline.

Recursion Crathes, Alba / Scotland, United Kingdom £41,000 – £52,000 pa

On-site Permanent