QUALIFICATIONS   Bachelor’s degree required. Degree in scientific field preferred. Master’s degree preferred. Minimum 8 years Data Management experience required including 3+ years team leadership  Demonstrated successful experience in all relevant clinical data management activities in a Biopharmaceutical or CRO setting  Working knowledge of all phases of clinical trials and ability to assess and determine study requirement from protocol review  Proficient experience using commercial clinical data management systems and/or EDC products (e.g.  Medidata RAVE, Oracle RDC / Inform, etc)  Knowledge of clinical research, FDA & ICH, GCP, GCDMP, and related regulatory requirements   Experience using relational databases (e.g. MS SQL Server, MS Access, or Oracle) and data visualization tools (e.g. Spotfire)  Familiarity with MedDRA/WHO-Drug coding   Knowledge of risk-based monitoring principles & associated analytics/metrics  Proven experience in vendor oversight to meet aggressive timelines of high-quality data deliverables  Strong Project and Risk Management Strong verbal and written communication in English skills; independently and effectively in multi-study, multi-disciplinary atmosphere in a matrix environment