iconplc - United States, IT - Administration, Remote work

Join a leading life sciences organization as a **Business System Adoption Specialist** in Blue Bell, PA. Leverage your 4+ years of experience in business analysis and change management to drive adoption of clinical trial systems like EDC. We seek a solution-oriented professional with strong prese...

Senior Clinical Research Associate (CRA) needed in Dallas or Houston, TX. Leverage your ophthalmology expertise to oversee multi-site trials, ensuring GCP and regulatory compliance. This role demands strong site management, data integrity, and travel (60%). Join ICON Plc for competitive benefits,...

Senior CRA opportunity in Philadelphia with ICON Plc. Manage clinical trial sites, ensure GCP and regulatory compliance, and drive data integrity. Requires a Bachelor's in a scientific field, extensive CRA experience, and strong site management skills. Enjoy competitive benefits including health ...

ICON plc seeks a Supplier Performance Monitor in Raleigh, NC, to oversee data quality and compliance for clinical trials. Ideal candidates possess laboratory auditing experience, with in-vitro diagnostics preferred, and relevant degrees plus 3-12 years of experience. This role involves monitoring...

Join ICON Plc as a Clinical Research Associate (CRA) in Oncology across multiple US locations. Leverage your advanced life sciences degree and extensive CRA experience to oversee trial sites, ensure GCP compliance, and manage data integrity. This role demands 60% travel and strong site management...

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...

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...