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Clinical Trials Data Manager
1 month ago
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 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 and 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.
- Supporting the production of regular reports (such as data entry and query progress of studies).
GHTU support:
- Preparing data management documentation and 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.
- Working closely with other members within GHTU to develop internal processes and training staff to ensure compliance and best practice adherence.
Qualifications and skills required:
- 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.
- Evidence of training in Good Clinical Practice.
- Programming experience in data management, such as MS Access, Excel.
- Programming experience in data management, such as MS SQL, SAS, Stata.
- 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
