Clinical Programmer I

Clinical Data Management support for assigned studies across DM sourcing models, including study startup/conduct/closeout activities, data quality oversight, and collaboration with study teams and external partners. Responsibilities include data review, user access testing, query management, data cleaning, data reconciliation with third parties, delivering study milestones, maintaining DM systems, ensuring audit-ready Trial Master File compliance, and supporting User Acceptance Testing of internal/external EDC systems. Requires a life sciences degree, fluent English, attention to detail, and ability to manage multiple projects in a global environment.