iconplc - Remote work

Join ICON plc in Mexico City as a Senior Clinical Data Science Programmer. Utilize your advanced SAS, R, or Python skills to develop programming solutions for clinical trial data analysis and reporting. You will ensure data accuracy and efficiency in a collaborative, cross-functional environment....

Lead clinical data science initiatives for a world-leading CRO. Ensure data quality and integrity across studies from setup to database lock. Requires 6+ years' lead experience, including study start-up and 5+ database locks. Competitive benefits and flexible location options in Johannesburg, Rea...

Join ICON plc, a global clinical research leader, as a Clinical Trial Associate in Raleigh or Blue Bell. Utilize your CRO/pharma experience to manage vendors and support study start-up activities. This role offers competitive benefits, including health insurance and retirement planning, in a dyna...

Join ICON plc as a Senior Clinical Research Associate (CRA) in Vienna. Oversee clinical trial activities, 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 insura...

Join ICON plc in Sao Paulo as a Senior Investigator Pricing Analyst. You will develop and analyze pricing strategies for clinical trial investigators, utilizing your financial analysis and modeling expertise. This role requires experience in cost management within healthcare or clinical research....

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 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...