iconplc - United States, IT - Administration, Remote work

Lead and coordinate clinical trial projects as a Trial Delivery Manager at ICON in Blue Bell, PA. We seek a seasoned project management professional with a Bachelor’s degree and proven leadership skills to deliver results on time and within budget. Drive cross-functional teams, manage stakeholder...

Senior Clinical Research Associate needed for Neurovascular trials in the Central/Midwest US. Monitor complex studies onsite or remotely, ensuring ICH-GCP and FDA compliance. Requires a BS in Life Sciences, 3+ years of CRO/pharma monitoring experience, and strong problem-solving skills. Enjoy com...

Senior Clinical Trial Manager (Oncology) – Home-Based, Blue Bell, US. Lead end-to-end trial management as a site-aligned partner, driving communication and issue resolution. Requires 3-5+ years of trial management, solid tumor oncology expertise, and ICH-GCP knowledge. Enjoy competitive benefits,...

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...

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...