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As a Clinical Research Associate at ICON, you'll independently set up and monitor clinical studies, prepare regulatory submissions, handle sponsor queries, and assist in training fellow CRAs while ensuring compliance with ICH-GCP guidelines.

The Senior Study Support Assistant will provide administrative and tracking support for study start-up processes. Responsibilities include assisting with submissions to regulatory authorities, updating tracking systems, maintaining electronic filing systems, coordinating meetings, and ensuring adherence to ICH GCP and ICON SOPs.

The CRA II is responsible for independently coordinating and monitoring clinical studies, ensuring compliance with ICON’s SOPs and regulatory standards. This role involves recruitment of investigators, preparation of regulatory submissions, conducting monitoring visits, maintaining study documentation, and ensuring timely reporting while motivating investigators to meet recruitment targets.

As a Clinical Research Associate II Specialist, you'll design and analyze clinical trials, ensuring compliance and data integrity while collaborating with investigators and site staff. Your role includes conducting site visits, performing data review, and preparing study documentation for innovative treatment advancements.

As a Study Start Up Associate II, you will oversee and ensure the site activation process for clinical trials meets sponsor timelines and requirements, engaging with site staff and supporting the use of ICON internal tools. You'll contribute to risk identification and project team discussions to enhance site activation efficiency.

The Supervisor of Finance will oversee the preparation of monthly management accounts, balance sheet reconciliations, and support statutory financial audits for multiple entities. They will lead and develop the finance team, ensure compliance with SOX and local legislation, and foster collaboration across financial and non-financial teams.

The In-House Clinical Research Associate will assist in planning and executing clinical trials, conduct site feasibility assessments, ensure compliance with study protocols, monitor study progress, and prepare study documentation. This role plays a key part in supporting the advancement of innovative treatments and therapies.