iconplc - United States, IT - Administration

Join ICON plc as a Senior Clinical Research Associate in the cardiovascular medical device space. This role requires deep FDA/ICH-GCP knowledge and strong site management skills for a key cardio/electrophysiology study. Enjoy competitive benefits and the flexibility of multiple US locations while...

Join ICON plc as a Senior Clinical Research Associate in the US, focusing on a cardiovascular medical device study. This role requires deep expertise in FDA/ICH-GCP guidelines and exceptional site management skills. We offer competitive benefits including health insurance and retirement planning,...

Join ICON plc as a Clinical Research Associate in Detroit, focusing on oncology trials. You will monitor sites, ensure GCP compliance, and manage data, traveling up to 50% in the Midwest. We seek a candidate with 2+ years of monitoring experience and oncology expertise. Enjoy competitive benefits...

Join ICON plc as a Senior Clinical Research Associate specializing in Orthopedics across the Western US. You will monitor 4-5 orthopedic device studies, ensuring compliance with FDA/ICH-GCP. This role requires strong site management and problem-solving skills. We offer competitive health insuranc...

Join ICON plc as a Clinical Research Associate in Miami, focusing on start-up activities across multiple therapeutic areas. You will identify and activate trial sites, ensuring compliance with ICH-GCP. This role requires 2-3 years of monitoring experience and offers competitive health insurance a...

Join ICON plc as a Clinical Research Associate in New Jersey. You will conduct on-site monitoring visits across the southeast, ensuring ICH-GCP compliance across key therapeutic areas like Oncology. This role requires 2+ years of monitoring experience and offers competitive benefits with up to 50...

Join ICON plc, a global clinical research leader, as a Clinical Research Associate II. You will monitor trial sites, ensure protocol/GCP compliance, and advance innovative therapies. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health insu...

Join ICON plc as a Clinical Research Associate II in Charlotte or Blue Bell. You will monitor clinical trial sites, ensure ICH-GCP compliance, and contribute to advancing treatments. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We offer competitive ...

Join ICON plc as a Senior Clinical Research Associate (CRA) in Houston, TX or St. Louis, MO. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Requires 5+ years of CRA experience, including oncology monitoring, and 60% travel. We offer competitive...

Join ICON plc as a Senior Clinical Research Associate in Oncology. Oversee clinical trials on the US West Coast, ensuring protocol compliance and data integrity. This role requires 5+ years of CRA experience with oncology monitoring and 60% travel. We offer competitive health insurance, retiremen...

Join ICON plc as a Senior Clinical Research Associate or CRA II in the United States. You will design and analyze clinical trials, ensuring protocol compliance and data integrity. This role requires 1-3+ years of independent monitoring experience, ICH-GCP knowledge, and 60% travel. We offer compe...

Join ICON plc as a Clinical Research Associate in the United States. You will monitor clinical trial sites, ensure ICH-GCP compliance, and contribute to advancing treatments. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We offer competitive health i...