Latest Project Services Jobs

Small Molecule CMC Leader - Senior Director

Leads Chemistry, Manufacturing and Controls (CMC) strategy and execution for small molecule, biopharm, or cell and gene therapy medicines from late-stage development through commercialisation. Oversees process development, regulatory filings, supply chain, and lifecycle management across global teams and external partners, ensuring readiness for approval and launch. Role involves high-level governance engagement, risk management, and transition to commercial supply.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent

Small Molecule CMC Leader - Senior Director

Lead CMC strategy and execution for small molecule drug development from Phase 2 through commercialization, managing cross-functional teams and global regulatory filings. Oversee tech transfer, process scale-up, and lifecycle planning while ensuring compliance with US, EU, and international standards. Interface with senior leaders and health authorities to drive successful product launches and post-approval activities.

GSK

Hybrid 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 relationships with biotech, academia, and investment networks. The Director will source and evaluate opportunities, lead deal teams, and represent CSL at industry events to enhance the company's reputation and deal flow.

CSL United Kingdom

Hybrid Permanent

Senior Director, Search & Evaluation Late TA Lead, Immunology

This role involves leading strategic sourcing and evaluation of late-stage external Hematology therapeutic area opportunities, from Phase 2 through marketed drugs. Responsibilities include engaging with Key Opinion Leaders, driving due diligence, and shaping the portfolio through high-impact partnerships.

CSL United States £263,000 – £328,000 pa

Hybrid Permanent

*Senior Clinical Development Medical Director - Renal

The Senior Clinical Development Medical Director will lead the strategy and execution of renal clinical development programs, from early to late phases. Responsibilities include providing clinical leadership, developing regulatory documents, ensuring patient safety, and collaborating with global teams and stakeholders.

Novartis London, United Kingdom

On-site Permanent

Medical Director, Gastroenterology, Early Clinical Development

This role involves leading global clinical trial teams through phase 1 and 2 development, drafting early clinical development plans, and serving as a medical lead for early clinical studies. The Medical Director will collaborate with biomarker experts, research scientists, and key opinion leaders to identify and implement strategies for preclinical and clinical support of gastroenterology programs.

Novartis London, United Kingdom

Hybrid Permanent

Senior Process Engineer

The Senior Process Engineer role at AstraZeneca involves developing and scaling up sustainable drug substance manufacturing processes. Responsibilities include introducing new equipment, optimizing processes, and collaborating with cross-functional teams to ensure robust and efficient production for clinical and preclinical trials.

AstraZeneca Macclesfield, United Kingdom

On-site Permanent

Senior Scientist, Translational PKPD

As a Senior Scientist in Translational PKPD Modeling & DMPK, you will apply your expertise in PKPD modeling and simulation to advance cancer biology understanding and accelerate drug discovery. You will provide specialist modeling input into pre-clinical projects, develop PKPD models, predict human dosing, and contribute to early clinical trials. This role involves cross-functional collaboration, strategic decision-making, and enhancing AstraZeneca’s translational research through publications and presentations.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Technical Program Coordinator, DDMR, London

As a Technical Program Coordinator, you will support the Drug Design and Medical Research (DDMR) function by managing program planning, monitoring timelines, tracking actions, and reporting risks. You will work closely with drug design teams, internal stakeholders, and external partners to ensure effective communication and alignment across the organization.

Isomorphic Labs London, United Kingdom

On-site Permanent

Technical Program Manager, ClinTech Strategy & Analytics

This role involves project managing and tracking the ClinTech roadmap, working closely with Clinical Development Operations and Decision Science to translate priorities into actionable plans. You will also support the communication of ClinTech’s progress to senior leadership and external audiences, contributing to vendor assessments and build-vs-buy evaluations. The role is at the heart of a high-visibility team building a platform to accelerate drug development.

Recursion North Tyneside, NE29 8EP, United Kingdom £136,200 – £211,100 pa

Hybrid Permanent

Head of Medicinal Chemistry, Drug Design, London

As Head of Medicinal Chemistry, you will lead a team of 25 chemists in London, driving the development of novel drugs using cutting-edge AI and machine learning. You will provide strategic direction, mentor team members, and collaborate with AI/ML scientists to accelerate drug discovery and clinical candidate nomination.

Isomorphic Labs London, United Kingdom

On-site Permanent

Supply Planner

The Supply Planner ensures uninterrupted production by managing raw material procurement and inventory across clinical and commercial manufacturing operations. This role involves running MRP processes, maintaining inventory policies, coordinating with suppliers and 3PLs, and leading supply continuity efforts. The position works cross-functionally with finance, quality, and manufacturing teams to align supply plans with demand forecasts and resolve supply chain disruptions.

Autolus Stevenage, United Kingdom

Hybrid Permanent

Principal Scientist, Bioanalytical & Molecular Assays

This role involves leading the development and validation of advanced molecular assays such as RT-qPCR, dPCR, and NGS to support clinical biomarker strategies across Moderna’s therapeutic pipeline. The scientist will work hands-on in assay design, optimization, and data interpretation, ensuring compliance with GCLP standards while integrating genomics, bioinformatics, and clinical insights. Collaboration with cross-functional teams is key to translating molecular data into actionable decisions for drug development.

Moderna Oxford, United Kingdom

Hybrid Permanent

Scientist, Clinical Biomarker Laboratory, Immuno-Assays - Cell Based

This role involves leading the development, qualification, and validation of cell-based immunoassays to support Moderna’s clinical trials across multiple therapeutic areas. The scientist will generate high-quality, GLP/GCP-compliant data from clinical samples, contribute to regulatory documentation, and collaborate with cross-functional teams and external partners. Emphasis is placed on scientific rigor, innovation in assay design, and mentoring junior staff within a regulated, collaborative laboratory environment.

Moderna Oxford, United Kingdom

Hybrid Permanent

Master Scheduler, Engineering

Work with usOur team are passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy and Autoimmune disease to deliver life-changing treatments to patients.Whilst working at Autolus you will enjoy a flexible, diverse and dynamic working...

Autolus Stevenage, United Kingdom