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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 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...

Lead clinical trials from planning to completion in a home-based role based in Seoul. Oversee timelines, budgets, and regulatory compliance while collaborating with cross-functional teams. This senior position requires a relevant degree, therapeutic expertise, and offers competitive benefits incl...

Join ICON plc as a Contract Analyst in Seoul. This home-based role involves preparing, verifying, and executing electronic invoicing for a client portfolio. We seek a finance or accounting graduate with strong analytical skills and attention to detail. Enjoy competitive benefits including health ...