(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...