- 5-7+ years experience in Clinical Data Management for pharmaceutical/biotech companies - need experience in all aspects of the DM lifecycle
- Strong vendor management experience - project managing and QCing CROs, data systems vendors etc
- Running multiple studies and project managing them at the same time
- Early phase (phase I) experience regarding clinical trial data is important
- Oncology, respiratory or pulmonary hypertension study experience preferred but not essential
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