Works collaboratively with Statistical Programmers, Biostatisticians, Global Drug Safety, Regulatory and Project Management staff to meet project deliverables and timelines for moderately complex clinical data acquisition, quality checking and reporting. Ensures completeness, correctness and consistency of clinical data and data structure across all projects. Responsibilities include: putting together highly effective CDM teams and delivering a clear sense of direction. Design and uses all available vehicles for effective scientific communication with and outside the company.