iconplc - IT - Software Development

ICON plc seeks a Project Manager, IRT to lead Interactive Response Technology solutions for global clinical trials in Sofia, Bulgaria. You will manage IRT system implementation, cross-functional teams, and project timelines within a leading healthcare intelligence organization. Ideal candidates b...

Join ICON plc as a CRA II in Seoul, South Korea, specializing in Oncology and Non-Oncology trials. Leverage 2+ years of clinical research experience and ICH-GCP expertise to conduct site monitoring, ensure data integrity, and advance innovative therapies. Enjoy benefits like health insurance, ret...

Senior Clinical Research Associate (Oncology) – Home-Based, Seoul, South Korea. Join ICON Strategic Solutions to lead global oncology SIT monitoring, ensuring GCP compliance and data integrity across multiple sites. Requires extensive CRA experience, strong site management skills, and 60% travel....

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...

Seeking a Clinical Trial Manager in Seoul, South Korea to drive clinical operations at ICON. You will manage study deliverables, ensure regulatory compliance, and collaborate with cross-functional teams. Requires a university degree in science/medicine and subject matter expertise. Enjoy competit...

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...

ICON plc seeks a Medical Data Reviewer in Warsaw, Poland. Leverage your Registered Nurse or life sciences background to ensure clinical data plausibility and consistency. You will independently draft Medical Data Review Plans and coordinate with Biometrics teams. Enjoy competitive benefits includ...

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...