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Clinical Data Manager

Job in Greater London, London, Greater London, W1B, England, UK
Listing for: Qureight
Full Time position
Listed on 2026-09-26
Job specializations:
  • IT/Tech
    Data Scientist, Data Analyst, Information Security & Data Protection
Salary/Wage Range or Industry Benchmark: 50000 - 70000 GBP Yearly GBP 50000.00 70000.00 YEAR
Job Description & How to Apply Below

About us

Qureight’s mission is to accelerate clinical trials and ensure breakthroughs in lung and heart disease reach patients without delay. Our AI-powered data and imaging curation platform enables the analysis of clinical imaging and other healthcare data, helping our customers bring treatments to market, faster.

We’re looking for talented people who want their work to matter. With offices in Cambridge and London, you’ll join our multidisciplinary team of clinicians, scientists, and engineers. What unites us is our open culture, continuous learning mindset, and a shared mission to help biopharma run faster, smarter trials.

At Qureight, we're building a company where data management is treated as a core capability, not an afterthought. Data management supports every imaging endpoint and biomarker we work with, in respiratory and cardiac trials where accuracy matters and the science is still developing. If you want complex datasets, are enthusiastic about being part of a growing team and clinical data that genuinely informs trial outcomes, we'd love to meet you.

About

the role

We are looking for a Clinical Data Manager to deliver compliant clinical data and image management activities for commercial (clinical study) projects. Bringing experience of clinical data management from clinical trials or imaging CROs, you will be responsible for image quality control, data and image transfers, user acceptance testing and for supporting continuous improvement as we develop our in-house clinical data management tooling and processes.

A positive, can-do attitude, and an understanding of clinical study data quality and regulatory standards is essential.

You will be responsible for working with...
  • Perform image (DICOM file) quality control activities (de-identification, visual screening etc.) in line with work instructions and best practice.
  • Raise data queries and support external and internal staff in their resolution.
  • Conduct data reconciliation activities and deliver image and data transfer packages to Sponsor and archival.
  • Support project/study managers in developing and agreeing data and image transfer specifications (agreements) with Sponsor, providing technical input where required.
  • Conduct user acceptance testing on project specific configurations of the Qureight Imaging Platform.
  • Be part of continuous improvement, suggesting and delivering revisions to work instructions and SOPs to develop best working practices in clinical data management relevant to Qureight.
  • Work with data engineers to support them in developing new and improved methods and tools for managing clinical and image data at Qureight.
  • Deliver activities on time and to a high standard across the board.
  • Conduct work in line with Qureight SOPs and in accordance with Good Clinical Practice (GCP) guidelines and all relevant regulations, including ISO
    27001 standards and data privacy regulations.
  • Build strong relationships with all stakeholders (with sponsors, with customers and within Qureight) maintaining transparent and consistent communication throughout.
What we need:
  • Minimum of two years of clinical data management experience, ideally in an imaging Clinical Research Organisation or Core Imaging Lab.
  • Experience working with technical teams and interacting via tools such as Jira.
  • Comfortable working with data via command line tools and scripts.
  • Demonstrated experience with clinical imaging related data (such as CT or MRI in DICOM formats) and/or other clinical variables.
  • Knowledge of PACS/VNA/AWS S3 Data Storage.
  • Demonstrated ability to cultivate and maintain key stakeholder relationships, both internally and externally.
  • Knowledge of ICH Good Clinical Practice (GCP) with evidence of recent training.
  • Track record of demonstrating a good attention to…
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