iconplc - Research and Development

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 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 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...

Join ICON plc as a Senior Clinical Research Associate (CRA) in Denmark, working remotely. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. This role requires extensive CRA experience, strong site management skills, and 60% travel. We offer compet...

Join ICON plc as a Clinical Research Associate II in Seoul. You will design trials, analyze complex medical data, and advance innovative therapies. Requires 2+ years of onsite monitoring experience and ICH-GCP knowledge. We offer competitive health insurance, retirement planning, and a supportive...

Join ICON plc as a Clinical Research Associate II in Bangkok. You will design trials, analyze medical data, and ensure protocol compliance and patient safety. Requires 2+ years of onsite monitoring experience and ICH-GCP knowledge. We offer competitive health insurance, retirement planning, and a...

Join ICON plc as a Senior Clinical Research Associate in Mechelen. Oversee clinical trials, ensuring protocol adherence, data integrity, and GCP compliance. Utilize your extensive CRA experience and monitoring expertise, with 60% travel. Enjoy competitive benefits including health insurance and a...