iconplc

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 ...

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...

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...