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The Senior Contract Analyst at ICON will manage contractual agreements, ensuring compliance and alignment with regulatory requirements. Responsibilities include drafting and negotiating contracts, analyzing contract terms for risks and opportunities, maintaining contract records, and developing contract management processes.

The Principal Statistical Programmer will lead and manage programming deliverables on multiple projects, ensuring quality and timely completion. Responsibilities include team management, client relationship development, implementation of technical solutions, and quality control of programming outputs.

As a Clinical Research Associate at ICON, you will oversee and coordinate clinical trials, ensuring compliance with regulations and safety protocols, while also collecting and analyzing critical data. Responsibilities include coordinating study activities, maintaining documentation, running queries, and developing stakeholder relationships.

As an Associate Project Manager, you will oversee client satisfaction by managing ICON Central Laboratories services, from the setup to daily operations of clinical studies. You will coordinate with sponsors and internal teams, ensure compliance with protocols, monitor study budgets, prepare management reports, and mentor junior team members.

The Client Relationship Manager at ICON will work with clients to assess needs, oversee client metrics, drive internal process improvements, and provide client training to enhance relationships. They will represent the organization in client meetings, troubleshoot quality issues, and communicate effectively with management and business development teams.

As a Senior Contract Analyst, you will manage contractual agreements, ensuring compliance and supporting project teams with contract interpretation and obligations. Your role includes reviewing, drafting, and negotiating contracts while maintaining organized records and improving contract management processes.

The Statistical Analyst will support clinical trial activities by contributing to study protocol development, statistical analysis plans, and related deliverables. Responsibilities include programming statistical procedures using SAS, creating complex macros, and communicating effectively with clients. The role requires strong analytical skills and attention to detail while working both independently and in teams.