Jobs at ICON plc

Lead centralized monitoring for clinical trials, oversee data-driven risk-based monitoring, ensure regulatory compliance, monitor site performance and patient safety, and coordinate cross-functional teams to improve trial quality and execution.

The Investigator Payments Coordinator supports the Investigator Payments team, managing payment processes, client communications, and ensuring accurate, timely investigator payments while maintaining compliance with standards.

The Financial Accountant I will manage financial transactions, prepare financial statements, ensure compliance with accounting standards, and support budgeting processes.

The Operations Engineer III will enhance EUC platforms, manage incidents, ensure security compliance, mentor junior staff, and support critical operations.

The Role involves overseeing finance workstreams, providing financial insights, budgeting, forecasting, and leading finance transformation initiatives, primarily utilizing Power BI for reporting and analytics.

The Manager, Statistical Programming leads a team in developing and validating statistical analysis solutions for clinical trials while ensuring quality and regulatory compliance.

The Senior Biostatistician will lead statistical analyses for clinical trials, mentor junior team members, and manage client interactions while ensuring compliance with regulatory standards.

The Senior Financial Accountant will lead reporting functions, design data models, implement controls, and deliver analytical reports. Responsibilities include collaboration with IT and stakeholders to create data solutions, ensure report accuracy, and provide insights to senior leadership.

The role involves developing and validating statistical programs for clinical trials, collaborating with teams on analysis, and mentoring junior programmers.

The Finance Analyst will manage project financial health, oversee setups in Oracle and P&F systems, maintain project information, prepare reports, and ensure compliance with internal controls.

The Site Specialist II manages site start-up and maintenance activities for clinical trials, ensuring compliance and smooth operations across teams.

The Logistics Analyst will analyze logistics data, optimize supply chain processes, collaborate with teams and vendors, and report on performance metrics.

As a Talent Acquisition Sourcing Specialist, you will attract talent, collaborate with hiring managers, maintain candidate pipelines, conduct screenings, and enhance sourcing processes.

Responsible for processing and payment of invoices, reconciliation of accounts, and resolution of supplier and employee queries.

The Database Developer II will design and maintain databases for clinical research projects, optimize data processes, and troubleshoot database issues.

The Investigator Pyts Coordinator will coordinate and ensure timely execution of investigator payments while supporting the payments team and clinical staff. Responsibilities include maintaining payment data and communication, conducting training, and escalating issues as necessary.

Lead and manage the execution of complex technical projects within the healthcare research sector, ensuring alignment with business objectives and effective team collaboration.

The Senior Analyst Engineer oversees analysis and optimization of engineering processes, collaborating on solutions, testing new technologies, and providing insights for decision-making.

The RBQM Manager leads risk-focused quality oversight in clinical studies, developing risk management planning, collaborating across functions, and driving RBQM strategies to ensure quality and compliance throughout the clinical trial lifecycle.

As a Senior Clinical Data Coordinator, you will design and analyze clinical trials, manage data flow, and mentor junior coordinators while ensuring compliance with standards.