Data Officer

**Minimum Requirements**:

- Bachelor of Arts Degree in Medical / Scientific / Biological / Statistical / Computer Science OR related field
- Valid GCP (Good Clinical Practice) Certificate
- 2 years relevant clinical trial experience
- Experience with statistical packages would be beneficial
- Excellent communication and interpersonal skills
- Detail-orientated, with strong organizational skills
- Proactive and able to work in a fast-paced environment
- Analytical and effective problem-solving skills

**Responsibilities include (but not limited to)**:

- Responsible for day-to-day collection of data activities, with the support of all other site staff.
- Ensure completeness, accuracy and consistency of the data to ensure quality standards expected for reporting to regulatory bodies, are met.
- Manage CRF’s and data flow; as well as ensure any updates to data collection form / CRF’s are distributed to study team
- Manage and supervise data entry for the current trial and training databases.
- Ensure accuracy of data in the systems through data integrity rules and designs in the database
- Check that all fields are completed, CRF’s signed and that correct version and page is used.
- Regular quality control of data entry reports
- Assist in raising source or CRF queries with relevant staff and review that these queries are resolved adequately.
- Extract daily data reports from data systems / study databases for statistical review, analysis and queries
- Ensure staff receive training on CRF’s and data entry applicable to the database
- The University of Cape Town Lung Institute is committed to equity in our employment practices and reserves the right not to appoint._

**Please Note: This Position is not on UCT Conditions of Service.**

Application Deadline: 2024/03/22