iconplc

Join ICON plc, a global clinical research leader, as a remote CRA II based in France. Utilize your 24+ months of independent monitoring experience on Phase II/III commercial trials. You will take full ownership of investigator sites, ensuring data integrity and compliance. We offer competitive be...

Join ICON plc as a Clinical Research Associate I/II in São Paulo. Oversee and coordinate clinical trials, ensuring ICH-GCP compliance and data integrity. This sponsor-dedicated role requires a science/medicine degree, excellent English, and 60% travel readiness. Enjoy health insurance, competitiv...

Join ICON plc as a Senior Clinical Research Associate (CRA) and shape the future of clinical development. Oversee trial activities, ensure protocol/GCP compliance, and manage site performance across multiple projects. This role requires extensive CRA experience, strong monitoring skills, and 60% ...

Join the world's largest CRO as a Senior Clinical Research Associate in Montreal. Utilize your 2+ years of on-site monitoring experience and ICH-GCP expertise to conduct clinical trial site visits. This role requires up to 60% travel and offers competitive health insurance and retirement benefits.

Join ICON Plc as a Senior Clinical Research Associate in Beijing or Guangzhou. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. This role requires extensive CRA experience, strong site management skills, and a willingness to travel 60%. We offer ...

Join ICON plc as a Senior Clinical Research Associate in Frankfurt/Mannheim. Oversee clinical trials, ensuring protocol adherence, data integrity, and GCP compliance. Requires extensive CRA experience, strong site management skills, and 60% travel. Enjoy competitive benefits including health insu...

Join ICON plc as a Clinical Research Associate I in Beijing. Oversee and coordinate clinical trials, ensuring ICH-GCP compliance and data integrity. This role requires a science/medicine degree, excellent English, and 60% travel readiness. We offer competitive health insurance, retirement plannin...

Join ICON plc as a Senior Clinical Research Associate in Beijing. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Requires extensive CRA experience, strong site management skills, and 60% travel. We offer competitive health insurance, retirement...

Join ICON plc, a global clinical research leader, as a Clinical Research Associate II in Kuala Lumpur. You will monitor sites, ensure protocol/GCP compliance, and contribute to advancing treatments. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel readin...

Join ICON plc as a Senior Clinical Research Associate (CRA) in the UK. Oversee clinical trial sites, ensuring protocol adherence, GCP, and data integrity. This role requires 3+ years' CRA experience, strong site management skills, and 60% travel. We offer competitive health insurance, retirement ...

Join ICON plc as a Pharmacovigilance Associate in Chennai. Process Clinical Trial cases using your LSMV database skills and 2+ years of PV experience. Ensure patient safety by analyzing adverse events and maintaining regulatory compliance. Enjoy competitive benefits including health insurance and...

Join ICON plc, a global clinical research leader, as an Accounts Receivable Associate in Chennai or Trivandrum. You will manage the full Contract-to-Cash billing cycle, ensuring accurate invoicing and compliance. The role requires 2-3 years' AR experience, outstanding Excel skills, and collaborat...