iconplc

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 Dietary Aid/Medical Research Representative in San Antonio. This PRN, day-shift role is vital for maintaining a clean, safe, and sanitized environment. Utilize your custodial skills and attention to detail in a supportive, innovative workplac...

Seeking a Manager for Data Monitoring Committee and Endpoint Adjudication projects. This role involves overseeing clinical trial projects, managing a team, and ensuring regulatory compliance with GCP/ICH guidelines. It offers a competitive benefits package and requires approximately 30% travel.

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 clinical data science programs at ICON in Blue Bell. Oversee complex data-driven projects from collection to insight implementation. Requires a strong background in data science, program management, and cross-functional leadership. We offer competitive health insurance, retirement plans, and...

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 as a Study Start-Up Associate and help shape the future of clinical development from home in France. You will facilitate clinical trial initiation, ensure regulatory compliance, and support document preparation. This role requires strong organizational skills and offers competitive ...

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 Local Trial Manager in Blue Bell, focusing on Oncology/Hematology trials. You will ensure end-to-end trial delivery, managing vendors and maintaining ICH-GCP compliance. This role requires 2+ years of local trial management and specific oncology experience. We offer competitive...

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 a global biotech leader in Perth as a Senior Clinical Research Associate. You will monitor early-phase Oncology/Haematology trials, ensuring GCP compliance and data integrity. This home-based role offers a competitive package, including health insurance and flexible leave, while you help adv...