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As a Senior Study Start Up Associate, you will drive study initiation by conducting feasibility assessments, negotiating site contracts, ensuring regulatory compliance, and safeguarding patient welfare through informed consent procedures.

The role involves managing and customizing CMS platforms, back-end development, UAT testing, portal setup and integration, and website analytics using Google Analytics 4. The developer will collaborate with a global team to deliver projects on time while having project management skills.

The IT Graduate Programme at ICON plc offers recent graduates the opportunity to rotate through various IT departments over two years, gaining critical experience in roles such as Cyber Security Analyst and IT Support Engineer, ultimately preparing them for future leadership within the clinical research industry.

As a Senior Clinical Research Associate, you will coordinate and monitor clinical studies, ensuring regulatory compliance and efficient study management. You'll prepare and evaluate study documentation, communicate effectively with team members, and manage onsite investigations while traveling extensively.

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.

ICON plc is seeking a Revenue Accountant to play a pivotal role in financial analysis and reporting related to clinical trials, contributing directly to the advancement of innovative treatments and therapies. Responsibilities include reviewing revenue recognition, collaborating with project teams, preparing accurate revenue schedules, and supporting external audits. The ideal candidate has a Bachelor's degree in accounting, finance, or related field, 2-5 years of experience in revenue accounting or financial analysis, strong understanding of revenue recognition principles, and proficiency in Microsoft Excel and ERP systems.

As a Clinical Research Associate at ICON, you will work with a team to set up and monitor clinical trials, complete reports, and ensure adherence to regulations. Key responsibilities include submitting ethical approvals, managing study documentation, and mentoring junior CRAs.