Jobs at ICON plc

As a CRA II, you'll conduct clinical trial visits, ensure protocol compliance, collaborate with site staff, and review clinical data.

In this role, you'll manage and process payments to clinical trial investigators, ensuring compliance and timely transactions while maintaining financial records.

As a Senior Programmer at ICON, you will develop and validate statistical programs for clinical trial analysis, collaborating with biostatisticians, ensuring data integrity, and mentoring junior team members.

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

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.

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 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.

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.

Manage negotiation, execution, and ongoing administration of clinical trial agreements and site budgets. Support site start-up, regulatory compliance, contract filing, risk escalation, and process improvements while collaborating with cross-functional teams and mentoring junior staff.

As a Treasury Analyst, you will manage cash flow, optimize financial resources, oversee bank relationships, and ensure compliance with regulations.

The Clinical Nurse Reviewer I supports clinical trial projects by reviewing documentation, ensuring quality and completeness, and managing communication between teams while adhering to clinical practices and regulations.

Prepare and maintain budgets, forecasts and P&L for business units; analyze monthly/quarterly results and KPIs; produce reporting packages and management presentations; support revenue pre-close, cost analysis, headcount management, and ad-hoc financial/business case analysis while partnering with project management.

The Investigator Payment Associate facilitates investigator payments, ensures compliance, resolves discrepancies, maintains documentation, and prepares financial reports.

The Manager, Finance role involves leading a finance team, managing revenue, improving margins, and providing financial insights for strategic decisions.

Lead the Investigator Forecasting team, ensuring delivery of accurate financial forecasts, partnering with Operations, and driving financial discipline and process improvements.

The Informed Consent Specialist develops, reviews, and ensures compliance of informed consent forms for clinical trials while collaborating with stakeholders and managing timelines.

The Software Engineering Manager will lead the development of technology solutions for clinical trial operations, manage software delivery, mentor engineers, and ensure compliance with healthcare regulations.

Lead implementation, optimization, and maintenance of clinical systems; collaborate with cross-functional teams to define requirements; monitor performance; provide training and stakeholder support to ensure data integrity and regulatory compliance.

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