iconplc - Remote work

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 Senior CTA and shape the future of clinical development. You will assist in designing and analyzing trials, interpret complex data, and advance innovative therapies. The role requires a scientific degree, clinical research experience, and excellent organizational skills. We off...

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 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 (CRA) in a home-based role in Germany. 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 ...

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 ...

Join ICON plc's dynamic team in Seoul as a Regulatory Affairs Specialist. You will design clinical trials, interpret medical data, and prepare key submissions (CT/IND, MAA/NA). This role requires 2-3 years of pharmaceutical regulatory experience. We offer competitive health insurance, retirement ...

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...