iconplc - United States, IT - Administration

Clinical Study Specialist role at ICON plc, a global leader in clinical research. Based in Warren NJ, Armonk NY, or Cambridge MA (hybrid). Requires a Bachelor’s degree and 2+ years industry experience supporting global trials with TMF, CTMS, and SharePoint. Enjoy competitive benefits, annual leav...

ICON seeks a Project Coordinator II in Blue Bell, PA, to drive project success through meticulous schedule management, documentation, and cross-functional communication. Ideal candidates possess a Bachelor’s degree or relevant experience, strong organizational skills, and proficiency in Microsoft...

Senior CRA (Oncology) sought for West Coast role at ICON, a world-leading clinical research organization. Leverage 5+ years of CRA experience with oncology monitoring expertise to manage multiple sites, ensure GCP compliance, and drive data integrity. This role offers extensive travel (60%) and r...

Join ICON as a Sr. TMF Specialist in Raleigh, NC, and ensure clinical trial document accuracy. Leverage 2+ years of TMF experience and a life sciences degree to manage document integrity, conduct audits, and support cross-functional teams. Enjoy benefits like health insurance, retirement planning...

Seeking a Clinical Study Lead in Boston, Basking Ridge, or Philadelphia. Leverage 5+ years of experience, including 3 years in management, to oversee CROs and vendors. Ensure protocol adherence, budget timelines, and strong site relationships. Enjoy competitive benefits, health insurance, and ret...

Senior CTA opportunity at ICON in the United States. Ensure clinical trial site compliance with GCP and regulatory standards. Requires a Bachelor’s in life sciences or clinical research, plus strong site management and analytical skills. Benefits include health insurance, retirement plans, life a...

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...

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 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...

Join ICON plc as a Local Trial Manager in Blue Bell, focusing on Oncology/Hematology trials. You will ensure end-to-end trial delivery, managing vendors and maintaining ICH-GCP compliance. This role requires 2+ years of local trial management and specific oncology experience. We offer competitive...