iconplc - Research and Development

Join ICON as a Clinical Research Associate II in Seoul, South Korea. Leverage 2+ years of CRA experience and ICH-GCP expertise to conduct site monitoring, ensure data integrity, and advance innovative therapies. Enjoy comprehensive benefits including health insurance, retirement planning, and glo...

Join ICON, a world-leading clinical research organization, as a Contract Senior Clinical Research Associate in Los Angeles. This 6-month role requires 3+ years of independent monitoring, ICH-GCP expertise, and 80% travel. You will oversee site visits, ensure protocol compliance, and drive data in...

Lead clinical trial oversight and site management as a Senior CRA with ICON Plc in Singapore. Utilize your extensive monitoring expertise to ensure protocol adherence, data integrity, and GCP compliance across multiple sites. This role offers competitive benefits and requires approximately 60% tr...

Join ICON plc, a global clinical research leader, as a Clinical Research Associate II in Singapore. You will design trials, analyze medical data, and ensure protocol compliance with 60% travel. Requires 2+ years CRA experience, ICH-GCP knowledge, and a life science degree. We offer competitive he...

Join ICON plc as a Senior Clinical Research Associate (CRA) in a home-based role in France. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and regulatory compliance. This role requires extensive CRA experience, Phase I Oncology expertise, and 60% travel. We offer ...

Join ICON plc, a global clinical research leader, as a Clinical Research Associate II in Shenyang. You will design and analyze trials, ensure protocol compliance, and advance innovative therapies. The role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitiv...

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

Lead clinical trial monitoring and site management in Prague as a Senior CRA for ICON Plc. Utilize your extensive CRA experience to ensure protocol adherence, GCP compliance, and data integrity across multiple sites. This role offers competitive benefits and involves approximately 60% travel. Dri...

Join ICON plc in Shanghai as a Clinical Research Associate (SSU). You will design trials, analyze complex medical data, and advance innovative therapies. We require 2+ years of CRA experience, ICH-GCP knowledge, and strong organizational skills. Enjoy competitive benefits including health insuran...

Join ICON plc as a Senior Clinical Research Associate in Milan. Oversee clinical trial activities, 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, re...

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 as a Clinical Research Associate II in Chengdu. You will monitor clinical trial sites, ensure protocol/GCP compliance, and manage data integrity. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel availability. We offer competitive health ins...