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As a Clinical Research Associate II Specialist, you will conduct site qualifications, monitor clinical trials, ensure compliance and data integrity, collaborate with investigators, and prepare study documentation.

As a Senior Clinical Research Associate, you will coordinate activities for setting up and monitoring clinical studies, ensuring compliance with ICH-GCP guidelines, preparing regulatory submissions, and mentoring less experienced CRAs. Travel is required up to 60% of the time.

The Biostatistician II position involves planning, monitoring, and organizing biostatistical activities for clinical studies. Responsibilities include protocol input, statistical analysis plan preparation, interpretation of data, and writing statistical sections of reports. The role encompasses leadership for moderate complexity studies and the ability to communicate effectively with clients.

As a Clinical Research Associate at ICON, you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate, and close-out investigational sites for clinical studies in phases II – IV, ensuring adherence to applicable regulations and principles of ICH-GCP.

As a Quality Assurance Auditor, you will perform internal audits, review GMP documentation, interpret regulations for GMP compliance, and facilitate client audits and inspections. You'll work with GMP manufacturing staff to ensure quality in early phase clinical research.

Senior Project Manager at ICON, responsible for overseeing projects and portfolios in the clinical research field. Primary liaison with clients, managing project deliverables, and providing leadership to project teams. Requires 5 years of clinical research experience.

The Senior Clinical Research Associate (CRA) identifies, selects, initiates, and closes out clinical study sites while ensuring compliance with study protocols and regulations. Responsibilities include monitoring, preparing documentation for ethics approvals, managing study queries, and possibly mentoring less experienced staff. Travel is required for site visits.