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Lead US clinical trials as a Local Study Associate Director at ICON plc. This role requires 5+ years of US trial management experience and deep ICH-GCP knowledge. You will oversee study commitments, lead local teams, and ensure regulatory compliance. We offer competitive health insurance, retirem...

Join ICON plc, a global clinical research leader, as a Clinical Study Coordinator in Salt Lake City. You will design trials, analyze medical data, and advance innovative therapies. The role requires a scientific degree, GCP knowledge, and strong organizational skills. We offer competitive benefit...

Join ICON plc as a Payment Analyst in Warsaw. Utilize your finance degree and 1-2 years' experience to ensure compliant investigator payments for clinical trials. You will process payments, resolve discrepancies, and streamline procedures in a dynamic, global environment. We offer competitive ben...

Join ICON as a Commercial Legal Counsel in Warsaw. Provide pragmatic legal advice and negotiate complex agreements for Pharma and Biotech clients. Leverage 2-5 years of in-house or law firm experience in commercial contracts. Enjoy competitive benefits including health insurance and a global supp...

Lead our Business Continuity Management in Ireland. Develop and implement robust continuity strategies, conduct risk assessments, and lead recovery planning. This hands-on role requires a CBCP/MBCP certification, 5+ years' experience, and a willingness to travel. We offer competitive benefits inc...

Leverage your clinical research expertise in a commercial role as a Business Development Associate at ICON plc. This role requires business-level French and offers a shift into sales, focusing on generating RFPs and building client relationships. Enjoy competitive benefits including health insura...

Join a global pharmaceutical leader as a Site Investigational Product Specialist in Reading, UK. Utilize your extensive clinical trial and IP administration expertise (IV, SC, IM) in Oncology/Immunology. Ensure safe investigational product preparation and serve as the key liaison between sponsor ...

Join ICON plc as an In-House CRA in Ankara. Utilize your life sciences degree and clinical research skills to support site management, document compliance, and data oversight. Enjoy a comprehensive benefits package while contributing to global clinical development in a collaborative, fast-paced e...

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

Join ICON plc as a Clinical Research Associate II in Mexico City. 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% domestic travel. We offer competiti...

Join ICON's AstraZeneca FSP program as a Global Clinical Trial Assistant. This home-based role requires 2+ years of global study support experience and ICH-GCP knowledge. You will manage the Trial Master File, coordinate study materials, and ensure regulatory compliance. We offer competitive heal...

Join ICON plc as a Senior Site Management Associate in Bucharest. Oversee clinical trial site operations, ensuring GCP compliance and high-quality data delivery. Requires extensive site management experience, fluency in Romanian, and strong problem-solving skills. We offer competitive health insu...