Latest IT Consulting Jobs

Associate Director, Clinical Operations Decision Analytics

Lead the development and deployment of data-driven analytics solutions to optimise clinical trial planning, execution, and resource allocation across global studies. Translate operational challenges into predictive models, dashboards, and decision-support tools while collaborating with cross-functional teams including clinical operations, data science, and technology. Mentor a team of analysts, ensure regulatory compliance, and drive the integration of analytics into operational workflows to improve trial efficiency and quality.

GSK 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 Director, R&D AI & Technology Portfolio

Lead strategic oversight and portfolio analytics for R&D AI and technology investments, providing data-driven insights to senior leadership. Drive decision-making through cross-functional collaboration, governance of the Technology Investment Board, and evaluation of build-vs-buy strategies. Focus on maximizing value, transparency, and delivery confidence across a complex, high-impact portfolio without direct program ownership.

GSK Stevenage, United Kingdom

Software Engineer (Data Services), London

This role involves building and maintaining scalable data services and platforms that support AI-driven drug discovery. You'll work closely with scientists and ML researchers to ingest, transform, and serve complex scientific data, enabling high-velocity research. The position requires strong backend engineering skills, particularly in Python and GCP, within a collaborative, interdisciplinary environment.

Isomorphic Labs London, United Kingdom

On-site Permanent

Medical Insights, Data Analyst Senior Manager

This role involves conducting ad hoc and exploratory data analysis to answer complex business and medical questions that cannot be addressed through existing platforms. The Senior Manager partners with global Medical Insights teams to translate ambiguous queries into actionable analytical approaches, validate datasets, and deliver clear, decision-ready insights. A key differentiator is the protected time for innovation—testing new data sources, AI methods, and proof-of-concept analyses to inform the strategic evolution of Pfizer’s global analytics platform.

Pfizer United States US$124,400 – US$207,400 pa

Medical Insights, Data Analyst Senior Manager

Performs ad hoc and exploratory data analysis to address complex business and medical questions that existing platforms cannot answer. Translates ambiguous queries into analytical approaches, validates datasets, and delivers clear, decision-ready insights to stakeholders in Medical Affairs. Also pilots new data sources, methods, and AI-driven techniques to inform future platform development and roadmap priorities.

Pfizer US$124,400 – US$207,400 pa

Connectivity Specialist

Evolve are partnering with a driven medical device manufacturer who are seeking a Connectivity Specialist to help shape the future of connected healthcare. This is an exciting opportunity to combine technical expertise, customer engagement, and project leadership to deliver innovative...

Evolve Selection Gloucester, Gloucestershire, United Kingdom

Head, PV and Regulatory QA

This role leads the global quality and compliance function for pharmacovigilance (PV) systems, ensuring adherence to international regulations and internal standards across clinical safety, regulatory affairs, and medical affairs. The position combines strategic oversight with hands-on operational leadership, including audit strategy, inspection readiness, deviation and CAPA management, and cross-functional GxP guidance. It requires deep technical expertise in PV processes and strong leadership to drive quality across global teams and third-party vendors.

CSL

Head, PV and Regulatory QA

Leads global pharmacovigilance and regulatory quality assurance, ensuring compliance with GVP, ICH, and regulatory standards across clinical safety, medical affairs, and regulatory affairs. Designs audit strategies, manages inspections, and oversees deviation management, CAPA, and change control systems. Provides cross-functional GxP expertise and drives continuous improvement in PV quality systems.

CSL

Director of Nonclinical Safety, Cambridge, MA

Lead the development and execution of nonclinical safety strategies for small molecule drug candidates in oncology and non-oncology programs, integrating AI-driven predictive models with traditional toxicology. Build and scale the nonclinical safety function within an AI-first drug discovery environment, ensuring high-quality data feedback to refine computational models. Collaborate across preclinical, clinical, and regulatory teams to advance compounds through IND and NDA/MAA-enabling studies.

Isomorphic Labs Cambridge, United Kingdom

Research Assistant in Microbial Genomics

This role involves managing and analysing a large collection of over 60,000 Neisseria gonorrhoeae genomes to study antimicrobial resistance, vaccine antigen diversity, and pathogen evolution. The postholder will develop and apply bioinformatics workflows for genome annotation, conduct population genomic analyses, and contribute to research dissemination through publications and presentations. Work will be conducted within a multidisciplinary team at the University of Oxford, with opportunities to support teaching and mentoring activities.

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

Contract

Quality Officer (GDP)

This role involves ensuring compliance with Good Distribution Practise (GDP), ISO 9001, and ISO 13485 standards through quality assurance activities such as managing deviations, change controls, audits, and supplier verifications. The Quality Officer will support the Quality Management System, conduct investigations, review documentation, and prepare for regulatory inspections. They will work closely with internal teams and external stakeholders to maintain product quality and process safety in a regulated environment.

Adecco United Kingdom

Hybrid Permanent

Field Service Engineer

Field Service Engineer - Medical & Aesthetic Laser SystemsSouth / South East England - Ideally located within London or the Home Counties£40,000 - £50,000 + Car AllowanceThe OpportunityI'm recruiting on behalf of a growing medical device service provider that partners...

Hunter Selection London, United Kingdom £40,000 – £50,000 pa

Clinical Development Director - Renal

The Clinical Development Director leads and supports clinical development activities within a global program, focusing on strategy, trial execution, data analysis, and regulatory documentation. This role involves close collaboration with cross-functional teams, ensuring scientific rigor and data quality across phases I–IV trials, particularly in late-phase development. The position requires strong scientific expertise, leadership in clinical operations, and active participation in safety and regulatory initiatives.

Novartis London, United Kingdom

Hybrid Permanent

Support Engineer

Provide first-line remote technical support for advanced diagnostic healthcare equipment, diagnosing faults and guiding customers through troubleshooting using remote tools like RDP, VNC, and augmented reality. Work in a fast-paced environment to resolve technical issues and ensure equipment remains operational, minimizing on-site visits while maintaining safety and customer service standards.

Quality Personnel Bradwell, Milton Keynes, Buckinghamshire, United Kingdom £37,500 pa