iconplc

Join Accellacare, part of ICON's network, as a Sr Clinical Research Nurse in Hickory, US. Autonomously coordinate and conduct clinical trial procedures, ensuring protocol compliance and patient care. Requires an RN/LPN license and strong GCP knowledge. Enjoy competitive benefits including health ...

Lead site contract negotiations for clinical trials across Poland, Bulgaria, Czechia, Ireland, or Romania. This homebased or office role requires 3-6 years of site contracts experience and expertise in Clinical Trial Agreements. Drive study timelines, ensure compliance, and mentor a team within a...

Join ICON plc as a Pharmacometrician and shape the future of clinical development. Utilize your expertise in NONMEM/Monolix to drive regulatory strategy and analysis plans. This role requires a PhD and 3+ years of applied model-based drug development experience. Enjoy competitive benefits includi...

Join ICON plc in Warsaw as a Local Trial Manager. Oversee the planning and execution of clinical trials, ensuring compliance with timelines, budgets, and regulations. Leverage your scientific degree and therapeutic expertise to lead cross-functional teams and manage site relationships. This role ...

Join ICON plc as a Clinical Research Associate II in Reading. You will conduct site monitoring visits, ensure ICH-GCP compliance, and contribute to innovative clinical trials. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We offer competitive benefit...

Join ICON plc as a Senior Clinical Research Associate in Basel. Oversee clinical trials, ensuring protocol adherence, data integrity, and GCP compliance across multiple sites. Requires extensive CRA experience, fluency in English, German, and French, and 60% travel. We offer competitive health in...

Join ICON plc as a Senior Clinical Research Associate in Ankara. Oversee clinical trials, 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, retirement ...

Join ICON plc as a Senior Clinical Research Associate in São Paulo. Oversee clinical trials, ensuring protocol adherence, data integrity, and GCP compliance. Requires extensive CRA experience, strong English, and 60% travel. We offer competitive health insurance, retirement plans, and global supp...

Join ICON plc as a Clinical Research Associate II in Puerto Rico. 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...

Lead advanced data science solutions for clinical trials at ICON plc. Utilize your expertise in SAS, R, or Python to ensure data integrity and support research. This senior role requires leadership skills and experience in clinical data programming. Enjoy competitive benefits including health ins...

Lead global clinical trial site activation as a Project Manager, ensuring timely, budget-conscious, and high-quality delivery. Utilize your 3-6 years of startup experience and regulatory knowledge to coordinate all activation activities. This role offers competitive benefits, including health ins...

Join ICON plc as a Clinical Research Associate II in Frankfurt. You will monitor clinical trial sites, ensure ICH-GCP compliance, and contribute to advancing treatments. The role requires 2+ years of CRA experience, fluency in English and German, and 60% travel. We offer competitive health insura...