iconplc - Remote work

Join ICON plc in São Paulo as a Clinical Research Associate I/II. 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, and 60% travel. We offer competitive h...

Join ICON plc as a Clinical Research Associate II in Sao Paulo. You will monitor clinical trial sites, ensure ICH-GCP compliance, and contribute to advancing treatments. This role requires a scientific degree, CRA experience, and 60% travel. We offer competitive health insurance and retirement pl...

Join ICON plc as an Investigator Payment Associate in São Paulo. You will ensure accurate, compliant financial processing for global clinical trials. This role requires a finance/accounting background and knowledge of regulations like the Sunshine Act. We offer competitive health insurance, retir...

Join ICON plc as a Clinical Research Associate II in São Paulo. 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 health insura...

Join ICON plc as a Clinical Research Lead Assistant and help shape the future of clinical development. This remote role requires strong organizational skills, fluency in English, and proficiency in Microsoft applications to provide key administrative support for clinical trials. We offer competit...

Lead global clinical trials from start-up to database lock as a Senior Clinical Trial Manager at ICON in Boston. Utilize your 10+ years of experience to oversee budgets, drive enrollment, and mentor CRAs. This pivotal role offers competitive health insurance, retirement planning, and a chance to ...

Join ICON plc in Budapest 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. We offer competitive health insurance, re...

Join ICON plc in Budapest as a Clinical Research Associate II. You will monitor clinical trial sites, ensure protocol/GCP compliance, and contribute to innovative therapies. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We offer competitive health in...

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 Singapore. Oversee and coordinate clinical trials, ensuring ICH-GCP compliance and data integrity. This role requires 2+ years of CRA monitoring experience, a relevant degree, and 60% travel readiness. We offer competitive health insurance, retire...

Join ICON plc as a Clinical Research Associate II in Ankara. 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 plans,...

Join ICON plc, a global clinical research leader, as a Clinical Research Associate II/Senior CRA in Belém do Pará. You will design trials, analyze complex medical data, and advance innovative therapies. We seek a degree holder with solid CRA experience in CRO/pharma and deep ICH-GCP knowledge. En...