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As a Statistical Programmer II, you will develop and validate statistical programs for clinical trials, ensuring data integrity and compliance. You will collaborate with teams, prepare statistical analysis plans, and mentor junior programmers.

The role involves developing and validating statistical programs, analyzing clinical trial data, and collaborating with biostatisticians to ensure accurate reporting and compliance with regulations.

The Financial Analyst II will lead financial report preparation, conduct variance analysis, maintain financial models, provide strategic guidance, and improve financial processes.

The Manager of Business Continuity will develop and implement strategies to ensure operational continuity during disruptions, assess risks, mentor team members, and lead recovery planning efforts.

Lead and support external audits for ICON, manage CAPA processes, and provide guidance on compliance with GCP and regulatory requirements.

The Manager, IT Operations oversees IT infrastructure management, drives process improvements, coordinates teams, and ensures operational efficiency while managing budgets and resources.

Develop and execute pharmacometric analysis plans, contribute to regulatory strategies, and align with multidisciplinary teams in drug development.

The Principal Clinical Data Science Lead oversees data management for clinical studies, ensuring data quality and compliance with standards, while managing CRO relationships and leading process improvements.

The Global Supply Chain Specialist will manage supply chain activities, analyze performance metrics, collaborate with teams, and ensure compliance with regulations.

The Business Development Associate will enhance market awareness and sales by managing RFPs, maintaining client relationships, and developing strategic sales initiatives.