iconplc - United States, IT - Administration, Remote work

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...

Join ICON plc as a Senior Clinical Research Associate in Ophthalmology. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and patient safety across multiple sites. This role requires extensive CRA experience, expertise in GCP, and 60% travel. We offer competitive hea...

Join ICON plc as a Senior Clinical Research Associate in Ophthalmology. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and patient safety across multiple sites. This role requires extensive CRA experience, strong monitoring skills, and 60% travel. We offer competi...

Join ICON plc as a Clinical Research Associate in the United States. You will monitor clinical trial sites, ensure protocol/GCP compliance, and manage data integrity. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health insurance, retiremen...

Join ICON plc as a Clinical Research Associate in Ophthalmology, based 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 of...