Latest Project Services Jobs

Principal Medical Writer

Author and lead the development of high-quality clinical regulatory documents such as protocols, Clinical Study Reports, and CTD submissions. Interpret complex clinical and statistical data to produce accurate, compliant narratives. Collaborate with cross-functional teams and manage complex writing projects across therapeutic areas and global submissions.

GSK CA$118,000 – CA$168,000 pa

Hybrid Permanent

Finance Portfolio Analytics Manager

This role involves building and leading the analytical framework for R&D investment decisions at a global biopharma company. The Finance Portfolio Analytics Manager designs financial models, valuation tools, and dashboards to translate scientific and clinical data into quantified financial impact. They lead strategic analyses, improve forecasting methodologies, and provide data-driven insights to senior leadership across complex portfolio decisions.

GSK

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

This role leads clinical development for Internal Medicine assets within Pfizer's Research & Development division, serving as the primary clinical accountability point for global regulatory submissions. The individual will direct cross-functional teams in designing and executing Phase 1-3 trials, develop clinical development plans, and contribute to regulatory filings, safety reports, and product labeling. The position emphasizes leadership in obesity-related therapeutics, digital innovation in clinical development, and engagement with external scientific and regulatory stakeholders.

Pfizer

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

This role involves leading clinical development for Internal Medicine assets within Pfizer's Research & Development division, with a focus on obesity and chronic weight management. The Global Development Lead is responsible for end-to-end clinical strategy, including designing and executing global clinical trials, regulatory submissions, and cross-functional team leadership. The position requires deep therapeutic expertise, strategic input into product development, and engagement with external stakeholders such as advisory boards and regulatory bodies.

Pfizer US$214,900 – US$358,100 pa

On-site Permanent

Security Engineering Manager, London or Lausanne

As a Security Engineering Manager, you will lead and scale a high-performing team responsible for securing Isomorphic Labs' AI-driven drug discovery platform. You'll define the technical security roadmap across cloud infrastructure, IAM, secure SDLC, and security monitoring, while enabling rapid innovation for ML researchers and drug discovery teams. The role involves pioneering AI-first security architectures, leading transformational projects, and acting as a key liaison within the Alphabet/Google ecosystem.

Isomorphic Labs United Kingdom

Associate Director, Clinical Program Management, Cambridge, MA

The Clinical Program Manager will lead the transition of internal drug programs from pre-IND stages into clinical trial execution, coordinating cross-functional global teams and managing timelines, budgets, and vendor partnerships. The role leverages AI and emerging technologies to drive efficient clinical development with a focus on high-probability outcomes. It involves strategic oversight of CROs and collaborators while ensuring alignment between clinical objectives and company goals.

Isomorphic Labs England

Hybrid Permanent

Associate Director, CMC Regulatory Affairs, International

This role involves leading CMC regulatory strategies and submissions for international markets, with a focus on mRNA-based products across vaccines, oncology, and rare diseases. The individual will guide global regulatory compliance, interact with health authorities, and support manufacturing and quality teams through regulatory interpretation and change control. It requires deep expertise in CTD-format filings and a proactive approach to managing multi-therapeutic regulatory programs in a fast-paced environment.

Moderna

On-site Permanent

Associate Director, CMC Regulatory Science, International

This role involves leading CMC regulatory strategy for global mRNA product development, preparing and reviewing regulatory submissions, and guiding cross-functional teams on compliance and agency interactions. The position requires deep expertise in biologics CMC regulations, particularly in EU and ROW markets, and plays a key part in shaping regulatory pathways across vaccines, oncology, and rare diseases. Based at the Harwell site, it emphasizes in-office collaboration within a multidisciplinary team.

Moderna

On-site Permanent

A

Senior Scientist Oncology Research

Conduct laboratory-based research to support immune-oncology drug discovery, focusing on developing and analysing in-vitro and ex-vivo assays to evaluate candidate therapeutics. Investigate mechanisms of action in tumour immunology using advanced immunological techniques and contribute to target validation. Work within a collaborative team environment in Cambridge, integrating scientific expertise with emerging data and technologies.

AstraZeneca Cambridge, United Kingdom

Contract

Mechanical Design Engineer

This role involves designing and improving machinery for industrial applications, focusing on detailed schematics, assembly drawings, and material specifications. The engineer will work on modernisation and refurbishment projects, ensuring compliance with UK and international standards. Key responsibilities include producing P&IDs, BOMs, and supporting manufacturing processes using CAD tools.

ASL Winchester, Hampshire, United Kingdom £40,000 – £50,000 pa

Senior Mechanical Design Engineer

This role involves leading mechanical design projects for industrial machinery, focusing on improvement, modernisation, and refurbishment of existing systems. The engineer will produce detailed schematics, assembly drawings, and BOMs while ensuring compliance with UK and international standards. Work includes cross-functional collaboration on process machinery used in sectors like pharmaceuticals, FMCG, and oil & gas, with occasional international travel for client site visits and training.

ASL Winchester, Hampshire, United Kingdom £45,000 – £55,000 pa

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Director, Data Scientist - Clinical AI

Lead the development and strategic implementation of AI methodologies for clinical trial design, biomarker discovery, and drug development across AstraZeneca's BioPharmaceuticals pipeline. Drive scientific innovation in collaboration with cross-functional teams, shape regulatory standards for AI in clinical evidence, and represent the company in external scientific forums. Focus on delivering reusable, enterprise-scale AI solutions grounded in rigorous data practices and translational impact.

AstraZeneca Cambridge, United Kingdom

Director, Clinical Pharmacology

Lead clinical pharmacology and pharmacometrics strategy across rare disease and oncology programs, designing studies and supporting regulatory submissions. Oversee modeling and simulation to inform dose selection and development decisions, working closely with cross-functional teams in a TechBio environment powered by AI-driven drug discovery. Serve as the primary expert in regulatory interactions related to clinical pharmacology.

Recursion London, United Kingdom £118,300 – £136,500 pa

Hybrid Permanent

Research Assistant in Proteomics

This role involves supporting proteomics research through sample preparation, operation of LC-MS/MS instrumentation, and analysis of proteomics data using statistical tools. The postholder will contribute to both laboratory workflows and data interpretation, maintaining quality control and supporting collaborative research projects across academic and clinical domains. Key responsibilities include managing sample tracking, generating reports, and helping develop targeted and untargeted mass spectrometry methods within a high-throughput, team-oriented environment.

University of Oxford Oxford, South East England, United Kingdom £35 – £41 pa

Contract

Electromechanical Engineer

Design and test electromechanical components for an FDA-regulated, point-of-care diagnostic device, including sensors, actuators, and integrated systems. Collaborate with software and systems engineers to develop a reliable, secure medical instrument, while improving test processes and evaluating emerging technologies. Work within a cross-functional team to drive innovation in a regulated environment with real-world clinical impact.

GxPeople Global Bath, Somerset, United Kingdom £60,000 – £70,000 pa