(Hybrid based in Bloemfontein, South Africa or Remote located in UK)
Your Tasks
You will lead study projects in the area of Clinical Data Management or represent and coordinate Metronomia project teams as project manager.
You represent Metronomia in project meetings with customers and study teams and, if desired, in other customer interactions (e.g. bid defense meetings).
You are actively involved in the clinical data management of clinical and non-interventional studies. This includes tasks in e CRF/e PRO setup and validation, DMP development, data review & cleaning and import of external data.
You design and conduct trainings for internal and external study teams in the area of Clinical Data Management.
You actively support the further development of the Clinical Data Management SOPs.
Your Profile
You have relevant training or a degree and at least 3 - 5 years of professional experience in Clinical Data Management in the pharmaceutical industry or a CRO.
Yo...