(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 eCRF/ePRO 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. You have a sound knowledge of GxP-regulated clinical research, clinical data management processes and CDISC standards. You are a team player with high social competence and very good communication skills. Our offer for you Appreciation and family-friendliness! We see and respect you as a person and support your professional compatibility with flexible working models. Excellence is worth it! We offer attractive remuneration and extensive company social benefits! Flat hierarchy! Our entire team meets at eye level at all times! In this way, we create a special working atmosphere for our highly motivated and qualified team! Challenging tasks! There is a detailed introduction to the area of responsibility and regular opportunities for internal and external training! #J-18808-Ljbffr