Latest IT Consulting Jobs

Medical Director, ViiV Healthcare

The Medical Director role at ViiV Healthcare involves managing and reporting data from Phase 1-4 clinical trials, contributing to the design and medical governance of studies, and providing medical expertise and support throughout the trial process. The role is crucial in advancing HIV treatments and working closely with internal and external stakeholders to ensure the success of clinical studies.

GSK

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 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

Data Management Specialist, London

As a Data Management Specialist, you will work closely with discovery project teams to integrate and curate high-quality experimental data, supporting the development of groundbreaking AI/ML models for drug discovery. Your role involves collaborating with internal and external teams to ensure data integrity and efficiency, contributing to the broader data team's efforts to build a robust data asset.

Isomorphic Labs London, United Kingdom

On-site Permanent

Data Curator, London

As a Data Curator at Isomorphic Labs, you will work closely with AI experts and drug discovery scientists to curate high-quality, ML-ready datasets. Your role involves integrating large-scale biomedical and biochemical data, enhancing data quality, and collaborating across teams to build and improve data assets that fuel the company's mission to accelerate drug discovery using AI.

Isomorphic Labs London, United Kingdom

On-site Permanent

Head of AI & Agentic Platform Engineering

This role leads the development and operation of Pfizer's core AI and agentic platform infrastructure, enabling enterprise-wide AI workloads across research, commercial, and supply functions. The leader will architect a scalable, secure, and governed platform supporting low-latency LLM inference, autonomous agent runtimes, model serving, and MLOps pipelines. It involves direct ownership of critical systems including the LLM gateway, agent orchestration, observability, and compliance infrastructure, with a strong focus on enabling rapid, safe deployment of AI models and agents in a regulated pharmaceutical environment.

Pfizer US$300,100 – US$500,100 pa

Hybrid Permanent

Head of AI & Agentic Platform Engineering

This role leads the development and operation of Pfizer's core AI and agentic platform infrastructure, enabling enterprise-wide AI execution across R&D, Commercial, and other functions. The leader is responsible for building a scalable, secure, and governed platform that supports both traditional ML workloads and next-generation autonomous AI agents, with a focus on stateful agent orchestration, low-latency inference, and full lifecycle governance. The platform enables rapid experimentation, deployment, and monitoring of AI systems in a highly regulated pharmaceutical environment.

Pfizer US$300,100 – US$500,100 pa

Hybrid Permanent Clearance Required

Senior Clinical Trial Case Manager

This role involves leading cross-functional teams in reviewing safety data, mentoring junior staff, and ensuring compliance with GxP guidelines and international regulations. The position also focuses on managing pharmacovigilance procedures, conducting impact assessments of new legislation, and supporting regulatory inspections and audits.

CSL

On-site Permanent

Director, QA Manufacturing

This role involves leading and developing the Front Line QA function at Seqirus Liverpool, ensuring pharmaceutical quality across all products. Responsibilities include providing 24/7 QA coverage, overseeing batch review and IT systems, and ensuring compliance with regulatory requirements. The role holder may also act as a QP, certifying and releasing products to market.

CSL United Kingdom

On-site Permanent

Band 6 Specialist Biomedical Scientist Haematology

As a Specialist Biomedical Scientist in Haematology and Blood Transfusion, you will work across central and satellite laboratories, processing and analysing patient samples, performing complex tests, and maintaining high standards of quality and safety. You will also support junior staff, manage stock, and participate in out-of-hours duties.

NHS Professionals Walton, Buckinghamshire, Buckinghamshire, HP21 7RY, United Kingdom £26 ph

On-site Permanent Clearance Required

Senior Scientist – AI and Computational Tools, Oncology R&D (12-Month

This role involves designing and deploying AI-powered tools and workflows for oncology research, building robust data infrastructure, and mentoring colleagues in computational methods. The Senior Scientist will work closely with wet-lab scientists, data science teams, and R&D IT to translate experimental data into scalable, reproducible systems.

AstraZeneca Cambridge, United Kingdom

On-site Contract

Clinical Study Administrator

As a Clinical Study Administrator, you will coordinate and manage the administrative aspects of clinical trials, ensuring that all documentation, regulatory submissions, and stakeholder communications are accurate and timely. You will work closely with various teams to maintain inspection readiness and support the smooth operation of multi-site studies.

AstraZeneca Chatham, ME4 4NP, United Kingdom

On-site Permanent

Regulatory Science Professional - Intelligence

This role involves managing regulatory intelligence for Roche’s pharmaceutical and medical device portfolio in the EU, with a focus on generating strategic, data-driven insights. The professional will leverage AI tools, maintain regulatory databases, and collaborate across global teams to inform decision-making and drive innovation in a dynamic regulatory environment.

Roche Welwyn Hatfield, United Kingdom

Hybrid Permanent

Sr. Engineer, Process Automation

The Role:Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.As Moderna continues to expand its presence in Harwell, this role...

Moderna Oxford, United Kingdom

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

Director, Regulatory Affairs

This role involves leading global regulatory strategy for drug development programs, managing regulatory submissions across all stages of development, and ensuring compliance with international health authorities. The Director will collaborate with cross-functional teams to identify regulatory risks, guide clinical development, and shape the future of regulatory science using innovative technology-driven approaches in a fast-paced TechBio environment.

Recursion North Tyneside, NE29 8EP, United Kingdom £207,500 – £280,720 pa

Remote Permanent