iconplc - IT - Administration

Senior CTA opportunity at ICON in the United States. Ensure clinical trial site compliance with GCP and regulatory standards. Requires a Bachelor’s in life sciences or clinical research, plus strong site management and analytical skills. Benefits include health insurance, retirement plans, life a...

Join ICON Plc as a Clinical Research Associate and oversee clinical trials across multiple US locations. Leverage your expertise in GCP, site management, and regulatory compliance to ensure data integrity and quality. This role requires a Bachelor’s in a scientific field, 60% travel, and strong p...

Join ICON plc as a Contracts Lead Investigator in Mexico City. You will review, negotiate, and manage clinical trial and vendor contracts, ensuring regulatory compliance. The role requires 2+ years of contract management experience, preferably in pharma or clinical research. We offer competitive ...

Lead Clinical Research Associate (CRA) specializing in Ophthalmology at ICON plc. Lead site management, mentor CRAs, and ensure ICH-GCP compliance across complex trials in the United States. Requires a life sciences degree and extensive CRO experience. Enjoy competitive benefits including health ...

ICON seeks a Clinical Research Associate II in Nanjing, China, to design and analyze clinical trials, ensuring protocol compliance and patient safety. Requires a Bachelor’s in science/healthcare, 2+ years CRA experience, and ICH-GCP knowledge. You will conduct site visits, manage data integrity, ...

Join ICON plc as a Site Management Associate II with French in Warsaw. Support clinical trial site management, ensuring GCP compliance and protocol adherence. Requires a Bachelor’s in life sciences, clinical research experience, and fluency in English and French. Enjoy benefits like annual leave,...

Join ICON plc as a Clinical Research Associate II in the United States. You will monitor clinical trial sites, ensure protocol/GCP compliance, and contribute to advancing innovative therapies. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive h...

Join ICON in Seoul as a Clinical Research Associate II. Design and analyze trials, ensuring protocol compliance and data integrity with ICH-GCP expertise. This role requires 2+ years of CRA experience and offers competitive benefits, including health insurance and global support. Expect approxima...

Join ICON plc as a Local Trial Manager in Blue Bell, focusing on Oncology/Hematology trials. You will ensure end-to-end trial delivery, managing vendors and maintaining ICH-GCP compliance. This role requires 2+ years of local trial management and specific oncology experience. We offer competitive...

Join ICON plc as a Senior Clinical Research Associate in Frankfurt. Oversee clinical trials, ensuring protocol adherence, data integrity, and GCP compliance. Requires extensive CRA experience, fluency in English & German, and 60% travel. Enjoy competitive health insurance, retirement planning, an...

Join ICON plc as a Senior Clinical Research Associate in Frankfurt. Oversee clinical trials, ensuring protocol adherence, ICH-GCP compliance, and data integrity. Utilize your 2+ years of CRA experience and fluency in German & English. Enjoy competitive benefits including health insurance and a gl...

Join ICON plc, a global clinical research leader, as a Senior Clinical Research Associate in Seoul, South Korea. You will oversee oncology trial sites, ensuring protocol adherence, data integrity, and GCP compliance. This role requires extensive CRA experience, strong site management skills, and ...