iconplc

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 ...

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...

Lead patient recruitment strategy for clinical trials in this remote US role. Utilize your 7+ years of experience and multi-channel expertise to drive enrollment. Enjoy competitive benefits while shaping the future of clinical development at a global leader.

Join ICON plc as a Study Start-Up CRA in Buenos Aires. You will oversee clinical trial sites, ensuring protocol adherence, GCP, and data integrity. We require extensive CRA experience, advanced English, and strong site management skills. Enjoy competitive benefits including health insurance and a...

Join ICON plc as a Clinical Site Associate (In-House CRA) in Hong Kong. Support clinical trial operations, ensuring site compliance and documentation accuracy in this hybrid office role. Utilize your life sciences background and organizational skills within a world-leading CRO. Enjoy competitive ...

Join ICON plc in Nanjing as a Clinical Research Associate II. Utilize your 2+ years of CRA experience and ICH-GCP knowledge to monitor sites and ensure data integrity in global clinical trials. This role offers significant travel, competitive benefits, and a chance to shape the future of clinical...

Lead the Accounts Receivable function for a global clinical research leader in Chennai. You will manage a team, optimize collections, and minimize delinquencies using your 5+ years of AR expertise. We offer competitive benefits including health insurance and a supportive, innovative environment.