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.

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

The Data Analyst I will perform image data reconciliation, ensuring accuracy between EDC and image data, while collaborating with teams and maintaining compliance.

The Pharmacovigilance Associate will monitor pharmaceutical safety by collecting and analyzing adverse event reports, ensuring regulatory compliance.

The Logistics Coordinator II will manage logistics activities for clinical trials, ensuring timely shipments while collaborating with cross-functional teams to meet compliance requirements.

The Senior Pharmacovigilance Associate manages and oversees pharmacovigilance activities, ensuring regulatory compliance, analyzing safety data, and mentoring junior staff.

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

As an Intern, you will assist in validating clinical applications, collaborate with teams to resolve issues, and maintain documentation following GCP standards.

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

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 activities for studies, analyze clinical trial data, mentor junior staff, and interact with clients and regulatory agencies.

As a Senior Statistical Programmer, you'll lead programming for clinical studies, develop ADaM datasets, mentor junior staff, and ensure compliance with quality standards.

Lead statistical strategy for Phase I-III oncology trials, mentor junior statisticians, perform data analysis using SAS and/or R, and ensure regulatory compliance.

The Informed Consent Specialist will develop and review ICFs, ensure compliance with regulations, collaborate with stakeholders, and manage timelines. The role includes mentorship and maintaining documentation accuracy.

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 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.