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As a Statistical Programmer II, you will be responsible for the statistical aspects of clinical and preclinical research projects, including study design, analysis planning, and data reporting. You will develop and document SAS programs, assist in protocol implementation, and support statisticians in their tasks while coordinating analysis efforts across multiple projects.

As a Clinical Research Associate II, you will conduct site qualification, initiation, monitoring, and close-out visits for clinical trials, ensuring compliance and patient safety. You'll collaborate with site staff, resolve data queries, and prepare study documentation to maintain high-quality clinical data.

As a Senior Clinical Research Associate, you will coordinate activities for clinical studies, ensuring compliance with ICH-GCP guidelines. Responsibilities include monitoring study progress, submitting necessary documents for ethics approval, preparing regulatory submissions, and possibly mentoring junior CRAs. The role involves travel for site monitoring and requires strong communication skills.

As a Clinical Research Associate II Specialist, you will conduct site visits for clinical trials, ensure compliance and data integrity, collaborate with staff, resolve data queries, and prepare study documentation. This role is pivotal in advancing innovative medical treatments.

As a Clinical Research Associate at ICON, responsibilities include setting up and monitoring studies, completing reports, submitting documents for approvals, and ensuring study cost efficiency. Requires at least 12 months of monitoring experience in clinical trials and a college degree in medicine or science.

As an HR Manager, you will oversee HR Consulting Services across multiple countries, collaborating with leadership on HR strategies, labor law compliance, and employee relations. Your role includes managing case advice, implementing HR initiatives, and analyzing HR data to drive improvements.

As a Senior Clinical Research Associate at ICON, you will independently coordinate and monitor clinical trials, ensuring compliance with regulations and preparing documentation. You will manage site activities, submit protocols for IRB approval, mentor junior CRAs, and balance sponsor queries while maintaining accurate status reports. Extensive travel is required for site monitoring.