iconplc - United States, IT - Administration

Senior Clinical Trial Manager (Oncology) – Home-Based, Blue Bell, US. Lead end-to-end trial management as a site-aligned partner, driving communication and issue resolution. Requires 3-5+ years of trial management, solid tumor oncology expertise, and ICH-GCP knowledge. Enjoy competitive benefits,...

ICON plc seeks a Clinical Research Associate II (XTA) in Chicago. Leverage 2+ years of on-site monitoring experience across multiple therapeutic areas. Ensure site compliance with ICH-GCP and manage visits using CTMS/eTMF. Enjoy competitive benefits, annual leave, and up to 50% travel across the ...

Join ICON as a Medical Research Associate in San Antonio. You will greet volunteers, check vitals, and support clinical trials with data collection and documentation. Requires a High School Diploma, medical assistant certification or allied health credential (e.g., EMT, LVN), and strong organizat...

Clinical Team Lead, Site Operations role in Hickory, US. Lead and mentor site operations staff, overseeing start-up, maintenance, and close-out tasks. Requires a Bachelor’s degree in life sciences or equivalent clinical research experience, plus strong leadership and GCP knowledge. Enjoy competit...

Join ICON plc as a Clinical Research Associate in multiple US locations. Leverage your onsite monitoring experience and ICH-GCP expertise to oversee oncology and multi-therapy trials. Enjoy competitive benefits, health insurance, and retirement plans while advancing innovative treatments. Travel ...

Join a leading life sciences organization as a **Business System Adoption Specialist** in Blue Bell, PA. Leverage your 4+ years of experience in business analysis and change management to drive adoption of clinical trial systems like EDC. We seek a solution-oriented professional with strong prese...

Senior Clinical Research Associate (CRA) needed in Dallas or Houston, TX. Leverage your ophthalmology expertise to oversee multi-site trials, ensuring GCP and regulatory compliance. This role demands strong site management, data integrity, and travel (60%). Join ICON Plc for competitive benefits,...

Senior CRA opportunity in Philadelphia with ICON Plc. Manage clinical trial sites, ensure GCP and regulatory compliance, and drive data integrity. Requires a Bachelor's in a scientific field, extensive CRA experience, and strong site management skills. Enjoy competitive benefits including health ...

Senior Clinical Research Associate opportunity in Raleigh, NC with ICON Plc. Manage and monitor clinical trial sites, ensuring GCP and regulatory compliance. Requires a Bachelor's in a scientific field, extensive CRA experience, and strong site management skills. Benefit from competitive health i...

ICON plc seeks a Supplier Performance Monitor in Raleigh, NC, to oversee data quality and compliance for clinical trials. Ideal candidates possess laboratory auditing experience, with in-vitro diagnostics preferred, and relevant degrees plus 3-12 years of experience. This role involves monitoring...

Join ICON Plc as a Clinical Research Associate (CRA) in Oncology across multiple US locations. Leverage your advanced life sciences degree and extensive CRA experience to oversee trial sites, ensure GCP compliance, and manage data integrity. This role demands 60% travel and strong site management...

Join ICON plc as a Clinical Study Specialist in Basking Ridge, NJ, supporting global trials across NA, LAM, EU, APAC, and India. Leverage your TMF, CTMS, and SharePoint expertise to organize reports, coordinate meetings, and review study documents. Requires a Bachelor’s degree and 2+ years of ind...