iconplc - Remote work

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

Join ICON plc as a Senior Clinical Research Associate in Seoul. Oversee global oncology trials, ensuring protocol adherence, data integrity, and GCP compliance. This role requires extensive CRA experience, strong site management skills, and 60% travel. We offer competitive health insurance, retir...

Join ICON plc as a Clinical Research Associate in Singapore. Oversee and coordinate clinical trials, ensuring ICH-GCP compliance and data integrity. This role requires 2+ years of CRA monitoring experience, a relevant degree, and 60% travel readiness. We offer competitive health insurance, retire...

Join ICON plc as a Clinical Research Associate II in Ankara. 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 plans,...

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 ...

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 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 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,...

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 ...

Lead and manage early-phase oncology clinical trials from planning through execution. This role requires strong ICH/GCP knowledge, Phase I oncology experience, and global vendor management skills. We offer a competitive benefits package including health insurance and retirement planning. This pos...