iconplc

Join ICON plc, a global clinical research leader, as a Contract Analyst I in Warsaw. Utilize your 5+ years of CRO/pharma contract negotiation experience to prepare and finalize clinical trial agreements and budgets. This role offers competitive benefits, including health insurance and retirement ...

Lead global clinical trial material (CTM) operations from Warsaw. This senior role requires 8+ years in clinical supply planning, vendor management, and cGMP/GCP. You will oversee packaging, inventory, and logistics, providing strategic supply chain leadership. We offer competitive health insuran...

Join the world's largest CRO as a Clinical Data Engineer in Livingston. Design and implement enterprise-level data pipelines for clinical trial integration using Python, SQL, and cloud platforms (AWS/Azure). Leverage 8+ years of experience to ensure high-quality data delivery for regulatory compl...

Join ICON plc as a Senior Statistical Programmer II in Reading, UK. Utilize your advanced SAS skills to analyze clinical trial data and ensure statistical integrity. Collaborate with biostatisticians in a dynamic team, contributing directly to vital clinical development programs. We offer competi...

Join ICON plc as a Senior Clinical Research Associate in Beijing or Guangzhou. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Utilize your extensive CRA experience and site management expertise in a world-leading CRO. Enjoy competitive benefits...

Join ICON plc as a Senior Clinical Research Associate in Sofia. You will manage Phase I-IV site monitoring and ensure regulatory compliance for a leading biopharma in cutting-edge therapies. This sponsor-dedicated role requires 3.5+ years of independent monitoring experience. We offer competitive...

Join ICON plc as a Senior Clinical Research Associate or CRA II in the United States. You will design and analyze clinical trials, ensure protocol compliance, and monitor sites with 60% travel. We require a scientific degree, 1-3+ years of independent monitoring experience, and ICH-GCP knowledge....

Join ICON plc as a Clinical Research Associate II in Wuhan, China. You will design and analyze clinical trials, ensuring protocol compliance and data integrity. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health insurance, retirement plan...

Join ICON plc as a Clinical Research Associate II in Guangzhou. You will monitor clinical trial sites, ensure protocol/GCP compliance, and manage data integrity. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health insurance, retirement pla...

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

Join ICON plc as a Clinical Research Associate II in Seoul. You will monitor global oncology trials, ensuring protocol compliance and data integrity with 60% travel. We require 2+ years of CRA experience, ICH-GCP knowledge, and SIT on-site monitoring expertise. Enjoy competitive health insurance,...

Join ICON plc, a global clinical research leader, in Seoul as a Senior Clinical Trial Associate. Utilize your CTA/CRA experience to manage essential documents, IMP, and safety data within our MAP programs. We seek a detail-oriented professional with strong communication skills and knowledge of tr...