iconplc - United States, Research and Development, Remote work

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...

Seeking an experienced Senior Clinical Research Associate (CRA) for oncology trials in the Midwest. You will monitor sites, ensure GCP compliance, and manage stakeholder relationships. This role offers competitive benefits including health insurance and requires extensive CRA experience with onco...

Join ICON plc as a Site Activation and Maintenance Associate I in Raleigh or Blue Bell. You will manage 25-30 sites, handling regulatory documents, IRB communication, and compliance. This role requires a Bachelor's degree and clinical research experience. We offer competitive health insurance, re...

Join ICON plc, a global clinical research leader, as a Clinical Trial Associate in Raleigh or Blue Bell. Utilize your CRO/pharma experience to manage vendors and support study start-up activities. This role offers competitive benefits, including health insurance and retirement planning, in a dyna...

Join ICON plc as a Senior Clinical Research Associate and help shape the future of clinical development. You will monitor sites, ensure protocol/GCP compliance, and contribute to innovative treatments. This role requires 9+ months of monitoring experience and 60% travel across the US. We offer co...

Join ICON plc as a Senior Clinical Research Associate (CRA) in a remote role based in Blue Bell, US. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. This position requires extensive CRA experience, strong site management skills, and 60% travel. ...