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    Liverpool, Liverpool, United Kingdom Lifelancer Full time

    Clinical Trials Data Manager Job DescriptionWe are seeking a highly skilled Clinical Trials Data Manager to join our team at Lifelancer. As a Clinical Trials Data Manager, you will play a critical role in the success of our clinical trials by ensuring the accuracy, integrity, and quality of our data.Key Responsibilities:Data Management: Provide data...

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    Liverpool, Liverpool, United Kingdom Lifelancer Full time

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    3 weeks ago

    Liverpool, Liverpool, United Kingdom Lifelancer Full time

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    1 week ago

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    Clinical Trials Data Management RoleAs a Clinical Trials Data Manager at Lifelancer, you will work closely with our team to ensure the smooth execution of clinical trials. Your responsibilities will include:Data Management: Providing input on CRFs, contributing to database development, and performing quality checks.Study Involvement: Liaising with...

  • Clinical Trials Data Manager

    2 weeks ago

    Liverpool, Liverpool, United Kingdom Lifelancer Full time

    As a Clinical Trials Data Manager, you will work closely with the GHTU team to ensure the smooth execution of clinical trials. Your responsibilities will include:General data management:Providing data management input on CRFs and contributing to the development of trial databases and eCRFs for studies.Performing QC checks and Database Quality Assessments on...

Clinical Trials Data Manager

2 months ago

Liverpool, Liverpool, United Kingdom Lifelancer Full time
Job Summary

We are seeking a highly skilled Clinical Trials Data Manager to join our team at Lifelancer. As a Clinical Trials Data Manager, you will play a critical role in the success of our clinical trials by ensuring the accuracy, integrity, and quality of clinical trial data.

Key Responsibilities
  • Data Management
    • Develop and implement data management plans for clinical trials
    • Design and develop clinical trial databases and electronic case report forms (eCRFs)
    • Perform quality control checks and database quality assessments
    • Monitor data for consistency and acceptability, and reconcile data from external sources
    • Extract and prepare data subsets for statistical analysis
  • Study Involvement
    • Liaise with chief investigators and statisticians to establish data management expectations
    • Assist study teams in monitoring participant data and developing trial documentation
    • Review, analyze, and validate clinical trial data to ensure consistency, integrity, and accuracy
    • Support the production of regular reports on data entry and query progress
  • GHTU Support
    • Prepare data management documentation and draft project-specific documents
    • Plan and track content, format, and quality of data management deliverables
    • Manage and update medical coding dictionaries
    • Work closely with other members to develop internal processes and train staff
Requirements
  • Bachelor's degree in a biomedical, scientific, statistical, or allied field
  • Strong self-sufficiency and initiative working with MSSQL databases
  • Evidence of training in Good Clinical Practice
  • Programming experience in data management, including MS Access, Excel, MS SQL, SAS, and Stata
  • Experience working in clinical trials, with a good understanding of CRF design and management
  • Experience developing reports using MSSQL scripts and Microsoft business reporting tools