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As a TMF Specialist at ICON, you will be responsible for completing Document Management activities in support of client services contracts and internal business needs. Tasks include processing study documents, maintaining study files, providing information for status reports, participating in audits, and liaising with clients and study teams. Strong communication skills and a Bachelor's degree in Life Science are required.

As a Principal Biostatistician at ICON, you will design and analyze clinical trials, interpret complex medical data, and lead statistical activities. Responsibilities include overseeing statistical processes, reviewing study protocols, preparing research proposals, and making presentations to clients.

As a Senior Clinical Research Associate, you will conduct site qualification, initiation, monitoring, and close-out visits for clinical trials, ensuring protocol compliance and data integrity. You will collaborate with site staff, perform data review, and contribute to study documentation preparation and review.

As an In-House Clinical Research Associate (IHCRA) at ICON, you will support the execution and management of clinical trials, conduct feasibility assessments, ensure compliance with study protocols, monitor study progress, and assist with documentation and reports.

The CRA II Specialist will conduct site visits for clinical trials, ensuring compliance and data integrity, collaborating with site staff, and reviewing study documentation. They will play a key role in the analysis and advancement of innovative treatments through their work on clinical trials.

The Clinical Research Associate II Specialist will conduct site visits for clinical trials, ensure compliance with protocols, maintain data integrity, and collaborate with site staff. They will also perform data review and assist in preparing study documentation.

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.