Opportunity Description
(Junior) Clinical Data Manager
(based in Bloemfontein, South Africa or Remote in UK)
Your Tasks
- Actively participate in Clinical Data Management for clinical and non-interventional studies, including tasks related to eCRF/ePRO setup and validation, DMP development, data review & cleaning, and importing external data.
- Support the ongoing development and improvement of Clinical Data Management Standard Operating Procedures (SOPs).
- You represent Metronomia in project meetings with clients and study teams.
- Manage documentation and maintain effective communication with study teams.
Your Profile
- You have relevant training or a degree and at least 1 - 2 years of professional experience in Clinical Data Management in the pharmaceutical industry or a CRO.
- You have a sound knowledge of GxP-regulated clinical research, clinical data management processes and CDISC standards...
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