iconplc - Remote work

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...

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...

Join ICON plc, a global clinical research leader, as a Clinical Research Associate II. You will monitor trial sites, ensure protocol/GCP compliance, and advance innovative therapies. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health insu...

Join ICON plc as a Clinical Research Associate II in Charlotte or Blue Bell. You will monitor clinical trial sites, ensure ICH-GCP compliance, and contribute to advancing treatments. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We offer competitive ...

Join ICON plc as a Senior Clinical Research Associate in Utrecht. Oversee clinical trials, ensuring protocol adherence, data integrity, and GCP compliance. Requires extensive CRA experience, fluency in Dutch/English, and 60% travel. Enjoy health insurance, competitive retirement plans, and a glob...