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Clinical Trials Data Coordinator

1 month ago

Liverpool, Liverpool, United Kingdom Lifelancer Full time
Clinical Trials Data Coordinator Job Description

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 clinical trial data.

Key Responsibilities:
  • Provide data management input on CRFs and contribute to the development of trial databases and eCRFs for studies.
  • Perform quality control checks and database quality assessments on clinical databases.
  • Monitor data for consistency and acceptability, reconciling data from external sources/relational databases.
  • Extract and prepare data subsets and derive variables for statistical analysis and follow procedures for the storage, archiving, and recovery of data.
Study Involvement:
  • Liaise with Chief/Principal investigators and statisticians to establish, align, and confirm data management expectations.
  • Assist study teams to monitor the status of participant data and help the team develop and review trial documentation related to data management.
  • Work with study teams to review, analyze, and validate clinical trial data to ensure consistency, integrity, and accuracy.
  • Support the production of regular reports (such as data entry and query progress of studies).
GHTU Support:
  • Prepare data management documentation and draft project-specific documents for trials (including Data Management Plans for grant applications).
  • Plan and track content, format, and quality of data management deliverables, including CRF design, data validation, data quality assessment, database lock, final datasets, and archiving.
  • Manage and update medical coding dictionaries, such as MedDRA and WHODrug.
  • Work closely with other members within GHTU to develop internal processes and train staff to ensure compliance and best practice adhered to.
Qualifications and Skills Required:
  • A degree or equivalent qualification in a biomedical/scientific/statistical or allied field or commensurate experience in clinical trial delivery.
  • Evidence of training in Good Clinical Practice.
  • Programming experience in data management, such as MS Access, Excel.
  • Experience of working in clinical trials with a particular experience of working with clinical data and a good understanding of CRF design and management.
  • Experience in developing reports using MSSQL scripts and Microsoft Business Reporting tools.

Please refer to the job description for full details on role responsibilities.