iconplc - IT - Software Development

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...

Join ICON plc in Shanghai as a Clinical Research Associate II. Leverage 2+ years of CRA experience and ICH-GCP expertise to conduct site monitoring, ensure data integrity, and drive clinical innovation. Enjoy benefits like health insurance, retirement planning, and global employee support. Advanc...

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...

Senior Clinical Python Programmer sought by ICON plc in Bangalore, India. Leverage 4+ years of experience in clinical data, Python, and SDTM to lead data science solutions for clinical trials. Drive innovation with PySpark, Spotfire, or Power BI in a dynamic, inclusive environment. Enjoy competit...

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 CRA II in Buenos Aires, Argentina, and drive clinical trial excellence. You will ensure protocol compliance, data integrity, and patient safety while conducting site visits. Requires a Bachelor’s degree, 2+ years of CRA experience, and ICH-GCP knowledge. Enjoy competitive benefits ...

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...

Senior CRA, home-based in Poland. Join ICON, a world-leading clinical research organization, to oversee trial activities ensuring GCP and regulatory compliance. Requires a Bachelor's in a scientific field, extensive CRA experience, and strong site management skills. Benefit from flexible work, he...

Join ICON plc as a Clinical Research Associate II in Seoul, South Korea. Leverage your 2+ years of SIT Phase I-III oncology monitoring experience to ensure protocol compliance and patient safety. Conduct site visits, collaborate with investigators, and uphold ICH-GCP standards. Enjoy competitive ...

Senior Clinical Research Associate (Oncology) – Home-Based, Seoul, South Korea. Join ICON Strategic Solutions to lead clinical trial monitoring, ensuring GCP and regulatory compliance across multiple sites. Leverage your CRA expertise in data integrity, site management, and stakeholder collaborat...