iconplc

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 Research Associate needed for Neurovascular trials in the Central/Midwest US. Monitor complex studies onsite or remotely, ensuring ICH-GCP and FDA compliance. Requires a BS in Life Sciences, 3+ years of CRO/pharma monitoring experience, and strong problem-solving skills. Enjoy com...

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 (Oncology) – Home-Based, Blue Bell, US. Lead end-to-end trial management as a site-aligned partner, driving communication and issue resolution. Requires 3-5+ years of trial management, solid tumor oncology expertise, and ICH-GCP knowledge. Enjoy competitive benefits,...

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...

ICON plc seeks a Clinical Supplies Project Manager to join its world-leading clinical research team in Warsaw or Gdansk, Poland. You will manage global supply planning, forecasting, and IRT system setup for clinical trials. Ideal candidates bring 4+ years of clinical supply experience, strong pro...

Lead clinical trials as Director, Clinical Operations at ICON in Sofia, Warsaw, Belfast, Poland, or Ireland. Drive performance, ensure GCP compliance, and manage cross-functional teams to advance innovative therapies. Requires a life sciences degree and extensive CRO/pharma experience. Enjoy comp...

Join ICON as a Study Support Assistant in Warsaw, Poland, and play a key role in advancing clinical trials. We seek candidates with a high school diploma (Bachelor’s preferred) and administrative experience, ideally in healthcare. You will manage study documents, coordinate meetings, and ensure r...

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...