iconplc - United States, IT - Administration, Remote work

Join ICON as a Site Management Associate I in Raleigh or Blue Bell, US. Support non-client sponsored studies, including Investigator Sponsored Studies, with a focus on operational execution and document tracking. Ideal for candidates with a scientific degree and clinical research experience. Enjo...

Lead global clinical trials as Manager, Clinical Operations at ICON plc in Raleigh, Charlotte, or Blue Bell, US. Leverage 5+ years of CRO/pharma experience and strong GCP knowledge to drive Phase 1-4 study strategies. Manage vendor relationships, budgets, and cross-functional teams with limited s...

ICON plc seeks a Feasibility Principal Analyst to lead strategic feasibility for rare disease programs across multiple US locations. This role requires 7+ years in clinical research with 5+ years of operational feasibility experience, translating complex enrollment data into actionable recommenda...

ICON seeks a Director, Research Services, Oncology to lead clinical research in Blue Bell, PA. This role drives protocol development, study start-up, and regulatory submissions (FDA/EMA) for solid tumor programs. Requires 8+ years oncology experience, a life sciences degree (Pharm.D./Ph.D. prefer...

Join ICON plc as a CRA II or Senior CRA in a home-based role across the U.S. (Portland, Salt Lake City, Houston, Downers Grove, Lawrence). You will independently monitor clinical trials, ensure ICH-GCP compliance, and safeguard data integrity. Requires a Bachelor’s degree, 1-3+ years of monitorin...

Senior Manager, Regulatory Strategy role in Raleigh, US. Leverage 7+ years of regulatory expertise to design clinical trials, develop submission plans, and advise ICON clients. Requires a Bachelor's in science/healthcare, supervisory experience, and strong strategic drug development skills. Benef...

Join ICON plc as a Clinical Associate (CTA) in Blue Bell, PA, and support cutting-edge clinical trials. Leverage your scientific degree and CRO experience to coordinate study activities, ensure regulatory compliance, and drive data accuracy. Enjoy competitive benefits including health insurance, ...

Seeking an experienced **Project and Portfolio Manager** in **Blue Bell, PA** to lead large-scale programs and cross-functional teams. You will drive complex projects from planning to delivery, managing budgets, resources, and risk. Requires a Bachelor’s degree, proven program management success,...

Senior Clinical Research Associate sought for a dynamic role at ICON, overseeing global trials with a focus on ophthalmology or gene therapy. Requires 5+ years of CRA experience, deep ICH-GCP knowledge, and 60% travel. Drive site management, ensure data integrity, and advance innovative treatment...

Join ICON as a Clinical Research Associate I in the United States. You will coordinate study setup, monitoring, and documentation while ensuring ICH-GCP compliance and patient safety. Requires a science degree, strong English communication, and 60% travel. Enjoy competitive benefits including hea...