Jobs 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.

Manages sales operations by analyzing performance, pipeline, forecasting, and market data; developing dashboards, reports, and forecasting models; improving sales processes and data governance; supporting commercial tools and systems; partnering with Sales, Finance, Business Development, and Operations leaders; leading continuous improvement; and coaching junior team members.

Manage, review, draft, negotiate, and analyze contracts for clinical research projects. The role identifies contractual risks, advises project teams on obligations and compliance, maintains contract records and deadlines, improves contract management processes, and mentors colleagues. Candidates need contract management experience in pharmaceutical, biotechnology, or clinical research settings, strong knowledge of contract law and regulatory requirements, excellent analytical and organizational skills, and willingness to travel approximately 5%.