Role Overview
In this role, you will support the management, quality control, and analysis of data collected through clinical trials and other health research studies. Your work will help study teams and oversight committees rely on accurate, timely information for monitoring progress, interpreting findings, and preparing research outputs.
Key Responsibilities
- Help develop study analysis plans and data management plans, and contribute to the design of databases suited to each study.
- Monitor data entry, run routine quality checks, identify missing or inconsistent information, and coordinate resolution of queries.
- Work with investigators, data clerks, data managers, and programmers to verify data and address issues in line with study protocols.
- Coordinate with trial teams and other data specialists to track data quality, missing records, reporting needs, and analysis timelines.
- Prepare progress reports and analyses for independent Data Monitoring Committees, Steering Committees, and research publications.
- Support interim and final analyses by producing summary tables and graphics, and discuss findings with study colleagues and collaborators.
- Track data-related milestones and deadlines, coordinating with internal staff and external collaborators to keep work on schedule.
- Prepare and archive research data and documentation for curation, ensuring data processes follow applicable data protection requirements.
Requirements & Qualifications
- Bachelor’s degree in Statistics, Biostatistics, Mathematics, Computer Science, or a related field from a recognized university.
- Knowledge of clinical trial data management and clinical database development.
- Working proficiency in at least one statistical package used for data handling and analysis, such as Stata, SPSS, SAS, or R.
- Experience with at least one database management tool, such as SQL Server or Microsoft Access.
- Strong analytical, planning, organizational, and detail-oriented working practices.
- Ability to work independently, manage competing tasks, and meet agreed deadlines.
- Clear communication and interpersonal skills, with the ability to contribute effectively in a multicultural team.
- One year of experience in data processing, management, or analysis within health or medical research is an advantage.
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