iconplc - Research and Development

Join ICON plc as a Clinical Research Associate (CRA) in Mechelen, Belgium. You will monitor clinical trial sites, ensuring protocol and GCP compliance. The role requires a life sciences degree, Dutch and English fluency, and proven monitoring experience. We offer competitive benefits including he...

Join ICON plc as a Clinical Research Associate II in Montreal. You will monitor clinical trial sites, ensure protocol/GCP compliance, and contribute to advancing new therapies. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health insurance,...

Join ICON plc as a Senior Clinical Research Associate in a remote role based in France. You will design and analyze clinical trials, ensuring protocol compliance and data integrity. This position requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health i...

Join ICON plc in Milan as a Clinical Research Associate II. You will design and analyze clinical trials, ensuring protocol compliance and data integrity. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health insurance, retirement planning, a...

Join ICON plc as a Clinical Research Associate II in Prague. You will monitor clinical trial sites, ensure protocol/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 insu...

Join ICON plc as a Senior Clinical Research Associate in Warsaw. 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 competitive health insurance, r...

Join ICON plc in Shanghai as a Clinical Research Associate II. You will monitor clinical trial sites, ensure protocol/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 in...

Join ICON plc as a Senior Clinical Research Associate in Paris. 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 competitive health insurance, re...

Join our dynamic team in San Antonio as a Medical Research Associate. Support clinical trial design, execution, and data management, ensuring accuracy and compliance. Ideal candidates have medical certification, strong organizational skills, and research software proficiency. We offer competitive...

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 Clinical Scientist I in Sao Paulo. Design and conduct pivotal clinical trials, applying your advanced life sciences degree and research experience. Collaborate with global teams to develop innovative therapies and enjoy comprehensive health and retirement benefits.