Bachelor’s degree or equivalent work experience preferred. 3+ years relevant experience in clinical/biomedical and/or software development environment preferred. 1+ years of experience working with at least 1 programming language (preferably SQL/SAS/Python/R) or any BI tool such as Tableau, Qlik, Power BI. Knowledge of Clinical Trial processes, specifically as they related to data collection, management, and preparation for statistical analysis. Good experience working with clinical trials in a data management-related role, or equivalent combination of education and experience. Ability to translate specifications into a cohesive demonstration. Ability to react to constructive criticism and remain neutral. Strong collaboration and team-building skills. Strong client facing and presentation skills. Self-motivating, able to assume responsibility and work autonomously in a professional manner. Excellent verbal and written communication skills, organizational and time management skills. Ability to think logically to solve complex problems. Experience in a similar role that requires a mix of technical and client-facing skills would be a plus. Strong understanding of clinical data systems to include collection sources such as EDC, CTMS, Safety, ePRO / eCOA, and other acquisition technologies. Ability to work with technical / engineering staff and translate new software features into real world examples. Experience demoing clinical systems such as EDC, CTMS, Analytics etc. Solid analytical and technical skills regarding software applications.