iconplc - United States, Research and Development

Senior Clinical Research Associate sought by ICON Plc to oversee global trial activities in Kansas City, MO. Requires advanced life sciences degree, extensive CRA experience, and 60% travel. Manage multiple sites, ensure GCP compliance, and drive data integrity. Benefits include health insurance,...

Senior CRA role at ICON: design and monitor clinical trials across multiple US locations. Requires 2+ years CRA experience, ICH-GCP expertise, and 60% travel. Responsibilities include site visits, data integrity, and protocol compliance. Benefits: health insurance, retirement planning, and global...

Join ICON, a world-leading clinical research organization, as a Contract Senior Clinical Research Associate in Los Angeles. This 6-month role requires 3+ years of independent monitoring, ICH-GCP expertise, and 80% travel. You will oversee site visits, ensure protocol compliance, and drive data in...

Join ICON as a Clinical Trial Liaison in Raleigh, USA. You will design and analyze oncology clinical trials, interpreting complex medical data. This role requires a life sciences degree and proven trial enrollment experience. We offer competitive health insurance, retirement plans, and a global s...

Join ICON plc, a global clinical research leader, as a Senior Clinical Research Associate in Oncology. This remote East Coast role requires 5+ years of monitoring experience, including site feasibility and start-up, with a focus on ICH-GCP. We offer competitive health insurance, retirement planni...

Lead study start-up for clinical trials at ICON in Blue Bell, ensuring regulatory compliance and efficient site activation. Manage a team and oversee the entire process from site identification to activation. This role requires extensive clinical trial start-up experience and strong leadership sk...

Join ICON plc, a global clinical research leader, as a Clinical Research Associate in Miami, FL. Utilize your 2+ years of monitoring experience and ICH-GCP expertise across diverse therapeutic areas. This role involves up to 50% travel for site management, offering competitive benefits including ...

Join ICON plc as a Clinical Research Associate (CRA) in the United States. Oversee multi-therapeutic area clinical trials, ensuring protocol adherence, GCP compliance, and data integrity. This role requires extensive CRA experience, strong site management skills, and 60% travel. We offer competit...

Join ICON plc as a Clinical Research Associate II or Senior CRA in a home-based U.S. role. You will independently monitor clinical trial sites, ensuring protocol compliance and data integrity with at least 60% travel. This position requires a scientific degree, 1-3+ years of monitoring experience...

Join ICON plc, a global leader in clinical research, as a Senior CRA or CRA II. You will design and analyze trials, ensure protocol compliance, and advance innovative therapies. The role requires 1-3+ years of monitoring experience, ICH-GCP knowledge, and 60% travel. We offer competitive health i...

Join ICON plc, a global healthcare intelligence leader, for a hands-on Summer Internship in Whitesboro, NY. Gain practical experience supporting clinical research projects while developing key professional skills. This full-time, onsite role is ideal for a current Bachelor's or Master's student s...