iconplc - Research and Development

Join ICON plc as a Clinical Research Associate in São Paulo. Oversee clinical trial activities, ensuring protocol and GCP compliance across multiple sites. This sponsor-dedicated role requires extensive CRA experience, strong site management skills, and 60% travel. We offer competitive health ins...

Lead patient recruitment strategies for clinical trials at ICON plc in Reading. Utilize your 7+ years of experience in clinical research and digital marketing to enhance patient access and engagement. You will analyze metrics, lead cross-functional teams, and build key partnerships. We offer comp...

Join ICON plc as a Clinical Supplies Manager in Warsaw. You will oversee clinical trial supply projects, ensuring regulatory compliance and timely delivery. This home-based role in Poland requires a relevant degree and proven pharmaceutical supply chain experience. We offer competitive health ins...

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

Join ICON Plc as a Senior Clinical Research Associate in Mannheim. Oversee clinical trial sites, ensuring protocol adherence, GCP, and data integrity. This role requires extensive CRA experience, strong site management skills, and 60% travel. We offer competitive health insurance, retirement plan...

Join ICON plc in São Paulo as a Senior Clinical Research Associate. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Utilize your extensive CRA experience and monitoring expertise, with 60% travel. Enjoy competitive health insurance, retirement p...

Join ICON plc as a Senior Clinical Research Associate (CRA) in the UK. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. This role requires extensive CRA experience, site management expertise, and domestic travel. We offer competitive benefits inc...

Join ICON plc as a Senior Clinical Research Associate and help shape the future of clinical development. You will monitor sites, ensure protocol/GCP compliance, and contribute to innovative treatments. This role requires 9+ months of monitoring experience and 60% travel across the US. We offer co...

Join ICON plc as a Senior Clinical Research Associate (CRA) in a remote role based in Blue Bell, US. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. This position requires extensive CRA experience, strong site management skills, and 60% travel. ...

Join ICON Plc as a Senior Clinical Research Associate in Mannheim. Oversee clinical trial sites, ensuring protocol adherence, GCP, and data integrity. This role requires extensive CRA experience, strong site management skills, and 60% travel. We offer competitive health insurance, retirement plan...

Join ICON plc as a Senior Clinical Research Associate in Helsinki. 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 insurance and ...

Seeking an experienced Senior CRA for oncology trials in the Southeast US. This role requires 5+ years of CRA experience with oncology monitoring and 60% travel. You will ensure protocol/GCP compliance, manage sites, and collaborate cross-functionally. We offer competitive health insurance, retir...