iconplc - Remote work

Join ICON Plc as a Clinical Research Associate and oversee clinical trials across multiple US locations. Leverage your expertise in GCP, site management, and regulatory compliance to ensure data integrity and quality. This role requires a Bachelor’s in a scientific field, 60% travel, and strong p...

Join ICON plc as a Contracts Lead Investigator in Mexico City. You will review, negotiate, and manage clinical trial and vendor contracts, ensuring regulatory compliance. The role requires 2+ years of contract management experience, preferably in pharma or clinical research. We offer competitive ...

Lead Clinical Research Associate (CRA) specializing in Ophthalmology at ICON plc. Lead site management, mentor CRAs, and ensure ICH-GCP compliance across complex trials in the United States. Requires a life sciences degree and extensive CRO experience. Enjoy competitive benefits including health ...

Join ICON plc as a Site Management Associate II with French in Warsaw. Support clinical trial site management, ensuring GCP compliance and protocol adherence. Requires a Bachelor’s in life sciences, clinical research experience, and fluency in English and French. Enjoy benefits like annual leave,...

Join ICON plc as a Clinical Research Associate II in the United States. You will monitor clinical trial sites, ensure protocol/GCP compliance, and contribute to advancing innovative therapies. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive h...

Lead clinical trial oversight and site management as a Senior CRA with ICON Plc in Singapore. Utilize your extensive monitoring expertise to ensure protocol adherence, data integrity, and GCP compliance across multiple sites. This role offers competitive benefits and requires approximately 60% tr...

Join ICON plc as a Senior Clinical Research Associate (CRA) in a home-based role in France. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and regulatory compliance. This role requires extensive CRA experience, Phase I Oncology expertise, and 60% travel. We offer ...

Join ICON plc as a Clinical Research Associate II in Kuala Lumpur. You will monitor clinical trial sites, ensure protocol/GCP compliance, and manage data integrity. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We offer competitive health insurance, ...

Join ICON plc as a Senior Clinical Research Associate in Milan. 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 insurance, re...

Join ICON as a Clinical Trial Liaison in Raleigh, USA. You will design and analyze oncology clinical trials, interpreting complex medical data. This role requires a life sciences degree and proven trial enrollment experience. We offer competitive health insurance, retirement plans, and a global s...

Join ICON plc, a global clinical research leader, as a Senior Clinical Research Associate in Oncology. This remote East Coast role requires 5+ years of monitoring experience, including site feasibility and start-up, with a focus on ICH-GCP. We offer competitive health insurance, retirement planni...

Lead clinical data science programs at ICON in Blue Bell. Oversee complex data-driven projects from collection to insight implementation. Requires a strong background in data science, program management, and cross-functional leadership. We offer competitive health insurance, retirement plans, and...