Education: - Diploma in Health related field - Essential Work Experience: - Experience in clinical research or laboratory setting - Preferred - Knowledge of ICH-GCP (Good Clinical Practice) guidelines - Preferred
- Assist with the development and execution of research studies and internal programs. - Assist, under instruction, with routing tests, experiments and procedures. - Provide assistance to research team to support on research methodology. - Organize data, files and other research study documents. - Collects, process, and assist in the compilation and verification of research data and samples. - Enter data from forms and documents into databases and other documents. - Assist with data verification and quality control, ensuring data integrity and consistency. - Provide assistance in tracking and managing data collection forms. - Perform other job related duties as required.
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