As a Clinical Data Coordinator I, you will assist in developing eCRFs, review clinical data, communicate with teams, and ensure study timelines are met.

The Image Data Processing Technologist will ensure compliance with regulations, verify data accuracy, and manage documentation in clinical research.

The Financial Accountant II will manage financial transactions, prepare financial statements, ensure accounting compliance, and support budget preparation.

The Financial Analyst II will provide financial and consulting services, assist in reporting, forecasting, budgeting, and developing financial plans for support departments.

As an Ops Support Analyst, you will provide support for IRT systems in clinical trials, assist with troubleshooting, and ensure data accuracy.

The Accounts Receivable Associate will manage invoicing for clients, ensure compliance with contracts, collaborate on audits, and build relationships with clients and internal teams.

The Senior Product Manager will lead end-to-end product delivery, collaborating across teams to align business needs with technology capabilities while ensuring continuous improvement and effective stakeholder engagement.

Develop and maintain programming solutions for clinical trial data analysis and reporting, ensuring accuracy and data quality while collaborating with teams.

Lead clinical data programming activities, oversee data quality, manage teams, and develop statistical analysis solutions for clinical trials.

Lead and mentor statistical programming teams, ensuring quality deliverables are met on time while supporting recruitment and operational activities.

As an Epidemiologist, you will design studies, perform analyses, prepare reports, and support client engagement while ensuring compliance with policies.

The Senior TMF Specialist will support the clinical development mission of ICON plc, focusing on operational excellence and compliance throughout clinical trials.

As an Informed Consent Specialist, you'll develop, review, and ensure compliance of informed consent forms for clinical trials, collaborating with stakeholders, managing timelines, and acting as a subject matter expert.

Lead and manage projects as a Senior Statistical Programmer, focusing on analysis, programming, and validating datasets with CDISC ADaM standards, while offering mentorship and support.

The Site Specialist II oversees clinical trial site operations including start-up, maintenance, and contract management, ensuring compliance and effective communication across teams.

The Senior Biostatistician will lead statistical analysis for clinical studies, develop analysis plans, and interpret medical data, contributing to innovative therapies.

The Senior TMF Specialist manages the Trial Master File for clinical trials, ensuring compliance with regulations, conducting checks, and collaborating with teams.