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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 adherence.
Qualifications and Skills:
  • 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.

Lifelancer is a talent 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