Teams at ICON plc

Manage Independent Data Monitoring Committee and endpoint adjudication projects for clinical trials. Responsibilities include planning schedules and budgets, coordinating innovation, data science, and technology teams, monitoring risks and progress, communicating with stakeholders, and supporting emerging technology integration. The role requires strong project management, organization, communication, and cross-functional collaboration skills, with endpoint adjudication experience preferred.

Coordinates clinical site contract execution, including routing agreements for signature, quality control, distribution, electronic filing, Medidata entry, reporting, and CDA negotiations. Serves as a liaison among investigative sites, vendors, legal teams, and internal stakeholders. Supports inspections and audits while maintaining accuracy, compliance, and effective communication in a cross-functional matrix environment.

Conducts site qualification, initiation, monitoring, and close-out for early-phase clinical trials across approximately three to four UK sites. Ensures patient safety, protocol compliance, data integrity, and regulatory adherence; reviews study data, resolves queries, identifies risks, and supports sponsors and study teams. Builds relationships with investigators and site staff while providing clinical research guidance and mentoring as appropriate.