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    {"title": "Clinical Trials Data Coordinator", "content": "Job SummaryWe are seeking a highly skilled Clinical Trials Data Coordinator to join our team at Lifelancer. As a key member of our team, you will be responsible for managing all aspects of clinical trial data, including data collection, validation, and analysis.Key ResponsibilitiesDevelop and...


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    {"title": "Clinical Trials Data Coordinator", "content": "Job SummaryWe are seeking a highly skilled Clinical Trials Data Coordinator to join our team at Lifelancer. As a key member of our team, you will be responsible for managing all aspects of clinical trial data, including data collection, validation, and analysis.Key ResponsibilitiesDevelop and...


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Clinical Trials Data Coordinator

2 months ago


Liverpool, Liverpool, United Kingdom Lifelancer Full time
Job Description

Clinical Trials Data Coordinator

We are seeking a highly skilled Clinical Trials Data Coordinator to join our team at Lifelancer. As a Clinical Trials Data Coordinator, 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
    • 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
  • Study Involvement
    • Liaise with 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 team members to develop internal processes and train staff
    Requirements
    • Qualifications
      • Bachelor's degree or equivalent in a biomedical, scientific, statistical, or allied field
      • Evidence of training in Good Clinical Practice
    • Skills
      • Programming experience in data management, such as MS Access and Excel
      • Experience working in clinical trials, with a focus on clinical data and CRF design and management
      • Experience developing reports using MSSQL scripts and Microsoft business reporting tools