iconplc - Remote work

Lead global clinical trial site activation as a Project Manager, ensuring timely, budget-conscious, and high-quality delivery. Utilize your 3-6 years of startup experience and regulatory knowledge to coordinate all activation activities. This role offers competitive benefits, including health ins...

Join ICON plc as a Clinical Research Associate II in Frankfurt. You will monitor clinical trial sites, ensure ICH-GCP compliance, and contribute to advancing treatments. The role requires 2+ years of CRA experience, fluency in English and German, and 60% travel. We offer competitive health insura...

Join ICON plc, a global clinical research leader, as a Clinical Research Associate II. You will monitor trial sites, ensure protocol/GCP compliance, and advance innovative therapies. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health insu...

Join ICON plc as a Clinical Research Associate II in Charlotte or Blue Bell. You will monitor clinical trial sites, ensure ICH-GCP compliance, and contribute to advancing treatments. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We offer competitive ...

Join ICON plc as a Senior Clinical Research Associate in Utrecht. Oversee clinical trials, ensuring protocol adherence, data integrity, and GCP compliance. Requires extensive CRA experience, fluency in Dutch/English, and 60% travel. Enjoy health insurance, competitive retirement plans, and a glob...

Join ICON plc as a Senior Clinical Research Associate (CRA) in Houston, TX or St. Louis, MO. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Requires 5+ years of CRA experience, including oncology monitoring, and 60% travel. We offer competitive...

Join ICON plc as a Clinical Research Associate II in Frankfurt. You will monitor clinical trial sites, ensure ICH-GCP compliance, and manage data integrity. This role requires 2+ years of CRA experience, fluency in English and German, and 60% travel. We offer competitive health insurance, retirem...

Join ICON plc as a Senior Clinical Research Associate in Oncology. Oversee clinical trials on the US West Coast, ensuring protocol compliance and data integrity. This role requires 5+ years of CRA experience with oncology monitoring and 60% travel. We offer competitive health insurance, retiremen...

Join ICON plc as a Senior Clinical Research Associate in Athens, Greece. Oversee oncology clinical trials, ensuring protocol adherence, data integrity, and GCP compliance. This role requires 12+ months of monitoring experience and offers extensive travel, competitive benefits, and a chance to sha...

Join ICON plc as a Senior Clinical Research Associate in Bangkok. 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, ...

Seeking a Senior Clinical Site Manager (CRA) for a part-time, home-based role in Melbourne or Sydney. This position requires extensive monitoring experience, GCP knowledge, and 50% travel. You will ensure protocol compliance and drive site performance for a leading pharmaceutical client. We offer...

Join ICON plc as a Clinical Research Associate II in a fully remote, FSP model role based in Frankfurt. You will monitor clinical trial sites, ensure ICH-GCP compliance, and contribute to advancing innovative therapies. This role requires 2+ years of CRA experience, strong organizational skills, ...