iconplc - IT - Software Development, Remote work

Join ICON as a Clinical Research Associate in Western Canada (Alberta, Vancouver, Burlington). Monitor Oncology studies in a sponsor-dedicated program, ensuring patient safety and regulatory compliance. Requires a science degree, ICH-GCP knowledge, and Oncology monitoring experience. Enjoy compet...

Join ICON as a Clinical Research Associate in São Paulo, Brazil. Leverage your ICH-GCP expertise and science degree to coordinate study setup, monitoring, and documentation. Ensure patient safety while managing sponsor queries and building strong site relationships. Enjoy benefits like health ins...

Join ICON as a Clinical Research Associate in Belém do Pará, Brazil. We seek experienced CRA professionals with a scientific degree and deep knowledge of ICH-GCP to conduct site monitoring and ensure data integrity. Enjoy benefits like health insurance, retirement planning, and global employee su...

Join ICON as a CRA I in Tel Aviv, Israel, and drive high-quality clinical trial monitoring. Leverage your ICH-GCP expertise and science degree to ensure patient safety and regulatory compliance. This role offers 60% travel, collaborative stakeholder engagement, and benefits like health insurance,...

Lead oncology clinical trials as a Trial Delivery Management Advanced at ICON in Burlington or Blue Bell, US. Drive project success with your extensive pharmaceutical project management expertise and leadership skills. Enjoy competitive benefits including health insurance, retirement planning, an...

Lead and coordinate immunology trial delivery as a Trial Delivery Management (Base) at ICON in Blue Bell, PA. This role requires a Bachelor’s degree and proven project management expertise, driving timelines, budgets, and cross-functional teams. Leverage PMP or PRINCE2 certifications to ensure qu...

Senior Clinical Research Associate needed for a cardiovascular/electrophysiology study (A-fib) with ICON plc. Ideal candidates bring 3+ years of monitoring experience and a Bachelor’s in Life Science, Nursing, or Biological Science. Cardiovascular medical device or pharma monitoring experience is...

Senior Clinical Trial Manager (Solid Tumor Oncology) – Home-Based, US. Lead end-to-end trial management with ICON, a world-leading CRO. Requires 3-5+ years oncology experience, ICH-GCP expertise, and strong site relationship skills. Enjoy competitive benefits, annual leave, and health insurance w...

Senior Clinical Trial Manager (LOM) – Hematology Oncology – Home Based (Blue Bell, US). Drive end-to-end trial management as a site-aligned partner, ensuring compliance with ICH-GCP and regulations. Leverage 3-5+ years of experience and hematology oncology expertise to streamline communication an...

Global Data Manager sought in Warsaw, Poland, to lead clinical data analysis and strategy for ICON. This role requires a Bachelor's degree in life sciences or computer science, extensive clinical data management experience, and strong leadership skills. You will oversee data governance, integrate...

Senior Clinical Research Associate (CRA) with oncology experience needed in Paris, France. Join ICON, a world-leading clinical research organization, to manage sites independently while ensuring ICH GCP and French regulatory compliance. Requires 4+ years of monitoring experience, fluency in Frenc...

Join ICON as a UK home-based Clinical Research Associate 1, specializing in In Vitro Diagnostics. This unique role offers a transition from lab-based work into clinical trial operations on a blue-chip diagnostics project. You will coordinate study initiation, monitoring, and completion while ensu...