Clinical Trials Data Analyst

3 weeks ago


Liverpool, Liverpool, United Kingdom Lifelancer Full time
Job Description:

As a Clinical Trials Data Manager, you will work in close partnership with the GHTU team in close communication with Chief/Principal Investigators and will be responsible for all aspects of the data management process, including development of project documentation, database setup, overseeing and supporting data collection and validation, data administration, archiving, and sharing.

Main Responsibilities:

  • Data Management: Providing data management input on CRFs, contributing to the development of trial databases and eCRFs for studies, performing QC checks and Database Quality Assessments on clinical databases, monitoring data for consistency and acceptability, reconciling data from external sources/relational databases, extracting and preparing data subsets and deriving variables for statistical analysis, and following procedures for the storage, archiving, and recovery of data.
  • Study Involvement: Liaising with Chief/Principal investigators and statisticians to establish, align, and confirm data management expectations, assisting study teams to monitor the status of participant data, helping the team develop and review trial documentation related to data management, working with study teams to review, analyze, and validate clinical trial data to ensure consistency, integrity, and accuracy, and supporting the production of regular reports (such as data entry and query progress of studies).
  • GHTU Support: Preparing data management documentation, drafting project-specific documents for trials (including Data Management Plans for grant applications), planning and tracking content, format, and quality of data management deliverables, including CRF design, data validation, data quality assessment, database lock, final datasets, and archiving, managing and updating medical coding dictionaries such as MedDRA and WHODrug, and working closely with other members within GHTU to develop internal processes and training staff to ensure compliance and best practice adhered to.

Requirements:

  • A degree or equivalent qualification in a biomedical/scientific/statistical or allied field or commensurate experience in clinical trial delivery.
  • Strong self-sufficiency and initiative working on MSSQL database, Data Manager.
  • Evidence of training in Good Clinical Practice.
  • Programming experience in data management, such as MS Access, Excel, MS SQL, SAS, Stata, etc.
  • Experience of working in clinical trials with 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.

Lifelancer is a length hiring platform in Life Sciences, Pharma, and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech, data science, and IT domains. Please use the below Lifelancer link for job application and quicker response.

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Remote Work: No



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