iconplc - IT - Administration

Join ICON plc as a Clinical Site Associate in Paris. Support clinical trial operations, ensure site compliance, and prepare for audits while building skills towards a CRA role. Requires a life sciences degree, fluency in French/English, and offers comprehensive benefits. This office-based positio...

Join ICON plc in Lisbon 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 insu...

Join ICON plc, a global clinical research leader, as a Senior Clinical Research Associate. This role requires 1-3+ years of monitoring experience, with oncology expertise preferred, and 70% travel. You will ensure trial compliance with ICH-GCP at sites across Canada, supported by comprehensive he...

Join ICON plc, a global clinical research leader, as a Senior CRA/CRA II. This home-based role in Melbourne, Sydney, or Brisbane partners you with a premier Biopharmaceutical company. You will monitor sites, ensure GCP compliance, and manage trials across a vast portfolio. The role requires exten...

Join ICON plc as a Clinical Research Associate II in Prague. 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, retire...

Join ICON plc in Seoul 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, ICH-GCP knowledge, and 60% travel. A competitive benefits package supports your...

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 Miami, focusing on start-up activities across multiple therapeutic areas. You will identify and activate trial sites, ensuring compliance with ICH-GCP. This role requires 2-3 years of monitoring experience and offers competitive health insurance a...

Advance your career as a Senior Clinical Research Associate with a global CRO leader. Utilize your oncology monitoring experience and ICH-GCP knowledge to drive clinical trials across Australia. This role offers significant travel, competitive benefits, and a chance to shape the future of clinica...

Join ICON plc as a Clinical Research Associate in Frankfurt. Oversee and coordinate clinical trials, ensuring ICH-GCP compliance and data integrity. This role requires a life sciences degree, fluency in English and German, and 60% travel. We offer health insurance, competitive retirement plans, a...

Join ICON plc as a Senior Clinical Research Associate (CRA) in a home-based role from Madrid. You will oversee clinical trial sites, ensuring protocol adherence, GCP compliance, and data integrity. This role requires extensive CRA experience, strong site management skills, and a willingness to tr...

Join ICON plc as a Senior Clinical Research Associate in Burlington, Canada. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Requires oncology monitoring experience and 60% travel. Enjoy health insurance, competitive retirement plans, and a supp...