iconplc - Remote work

Join ICON as a Site Management Associate I in São Paulo, Brazil. Support clinical trial site monitoring, ensure GCP compliance, and manage documentation. Ideal for candidates with a Bachelor’s in life sciences or clinical research and strong organizational skills. Enjoy benefits like annual leave...

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...

Lead oncology clinical trials as a Trial Delivery Management Advanced at ICON in Burlington or Blue Bell, US. Drive project success with your extensive pharmaceutical project management expertise and leadership skills. Enjoy competitive benefits including health insurance, retirement planning, an...

Lead and coordinate immunology trial delivery as a Trial Delivery Management (Base) at ICON in Blue Bell, PA. This role requires a Bachelor’s degree and proven project management expertise, driving timelines, budgets, and cross-functional teams. Leverage PMP or PRINCE2 certifications to ensure qu...

Join ICON plc as a Contract Associate in Madrid, Spain. Leverage your 2+ years of contract management experience and law/business degree to draft, negotiate, and manage agreements in a world-leading clinical research organization. Enjoy home-based flexibility, comprehensive health insurance, reti...

Join ICON as a Graduate Pharmacovigilance Associate in Warsaw, Poland. Support global drug safety by collecting and processing adverse event data, preparing regulatory reports, and collaborating with cross-functional teams. Ideal for life science or pharmacy graduates with strong attention to det...

Senior Clinical Research Associate needed for a cardiovascular/electrophysiology study (A-fib) with ICON plc. Ideal candidates bring 3+ years of monitoring experience and a Bachelor’s in Life Science, Nursing, or Biological Science. Cardiovascular medical device or pharma monitoring experience is...

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 (Solid Tumor Oncology) – Home-Based, US. Lead end-to-end trial management with ICON, a world-leading CRO. Requires 3-5+ years oncology experience, ICH-GCP expertise, and strong site relationship skills. Enjoy competitive benefits, annual leave, and health insurance w...

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,...

Senior Clinical Trial Manager (LOM) – Hematology Oncology – Home Based (Blue Bell, US). Drive end-to-end trial management as a site-aligned partner, ensuring compliance with ICH-GCP and regulations. Leverage 3-5+ years of experience and hematology oncology expertise to streamline communication an...

Global Data Manager sought in Warsaw, Poland, to lead clinical data analysis and strategy for ICON. This role requires a Bachelor's degree in life sciences or computer science, extensive clinical data management experience, and strong leadership skills. You will oversee data governance, integrate...