Latest Managed Services Jobs

Global Medical Director - Specialty Care

This role involves designing and implementing a global framework for Medical Science Liaison (MSL) teams, ensuring alignment across regions and markets. The position focuses on governance, performance metrics, and operational execution to enhance clinical trial engagement and scientific exchange with investigators and KOLs. It requires strategic leadership, cross-functional collaboration, and a strong understanding of medical affairs in a global biopharma context.

GSK United Kingdom

Global Medical Director - Specialty Care

Leads the design and implementation of a global Medical Science Liaison (MSL) framework, focusing on governance, deployment models, and performance metrics across markets. Works cross-functionally to align medical, R&D, and regional teams, ensuring consistent scientific engagement with investigators and KOLs in support of clinical trials. Focuses on operational excellence, change enablement, and strategic evolution of field medical models in respiratory and hepatology therapeutic areas.

GSK

Manager, Statistics

Leads statistical design and analysis for clinical trials and observational studies, ensuring scientific rigor and regulatory compliance. Collaborates across functions to support drug development, regulatory submissions, and evidence generation using clinical and real-world data. Contributes to methodology research and maintains best practices within Pfizer's statistics community.

Pfizer United Kingdom

Clinical Development Medical Senior Manager

This role involves leading the medical and scientific oversight of clinical trials, ensuring protocol integrity, participant safety, and high-quality data review. The Senior Manager will apply AI-enabled tools and digital approaches to enhance trial design, execution, and risk management. Responsibilities include medical monitoring, safety data analysis, supporting regulatory filings, and contributing to clinical study reports and publications.

Pfizer Sandwich, United Kingdom

Head of Medicinal Chemistry, Drug Design, London

Lead and strategically guide a team of 25 medicinal chemists in redefining drug discovery through deep integration with AI and machine learning. Shape the scientific direction of projects from hit identification to candidate nomination, while fostering collaboration across computational design, biology, and pre-clinical development teams. Drive innovation by challenging traditional paradigms and embedding an AI-first culture across the chemistry function.

Isomorphic Labs London, United Kingdom

On-site Permanent

Senior Project Specialist, Clinical Supplies

This role involves managing end-to-end clinical supply operations for Moderna’s mRNA-based therapeutic trials, including coordination of labeling, packaging, distribution, and temperature-controlled logistics. The specialist ensures investigational products are delivered on time and compliantly to clinical sites, supports IRT system testing, monitors vendor performance, and drives digital innovation and process improvements in supply chain execution.

Moderna

Hybrid Permanent

(Fixed Term) Warehouse Specialist

Operate within a GMP-regulated warehouse environment at Moderna’s Harwell site, managing inbound and outbound material flows, inventory control via SAP, and supporting continuous mRNA manufacturing operations. Perform cycle counts, documentation, and logistics coordination while adhering to strict quality and safety standards. Gain exposure to digital-first and AI-enabled tools within a fast-paced, collaborative pharmaceutical setting.

Moderna

Software Engineer (TechOps), London

This role involves building and managing cloud infrastructure and DevOps tooling to support AI-driven drug discovery. You'll work across research, development, and production environments using GCP, Kubernetes, and Infrastructure as Code, collaborating closely with scientists, ML researchers, and engineers. The focus is on creating scalable, secure, and automated systems that accelerate scientific innovation in a fast-moving, interdisciplinary environment.

Isomorphic Labs United Kingdom

Hybrid Permanent

Global Regulatory Associate Director, Life Cycle Management

Manages regulatory maintenance for a high-complexity pharmaceutical portfolio, ensuring compliance and timely submissions. Develops strategic regulatory input for safety reports, variations, and renewals, while acting as a liaison with health authorities. Supports global approval processes and contributes to process improvements and team mentorship.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

Associate Director, Statistical Programming

Lead a global team of statistical programmers, driving standardization, innovation, and quality in clinical trial data analysis. Develop programming strategies using modern tools like R, Git, and AI-enabled technologies, ensuring audit-ready deliverables and alignment with biostatistics and data management. Provide technical leadership and influence global drug development strategy across phases I–IV studies.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

Manufacturing Operator I - Night Shift

Operate in a cGMP cleanroom environment to assemble, inspect, and package single-use medical devices using technical drawings and hand tools. Perform quality checks and maintain accurate batch records in compliance with strict manufacturing standards. Work on a 4-on/4-off night shift pattern in a highly regulated healthcare setting.

Randstad Construction & Property Cramlington, Northumberland, United Kingdom £13 – £13 ph

Test Engineer

This role involves designing and implementing quality test procedures for both software and hardware components of medical devices. Responsibilities include attending design meetings, writing test plans, analyzing opportunities for automated testing, and ensuring compliance with regulatory standards.

Quality Start Walsall, West Midlands (county), United Kingdom £30,000 – £35,000 pa

On-site Permanent

Test Quality Assurance Engineer

This role involves designing and implementing quality test procedures for both software and hardware in medical device products. Responsibilities include attending design meetings, writing test plans, and ensuring compliance with regulatory standards.

Quality Start Walsall, West Midlands (county), United Kingdom £30,000 – £35,000 pa

On-site Permanent

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