iconplc - IT - Administration

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...

Join ICON plc as a Clinical Research Associate II in Paris, France. This FSP role offers hybrid or home-based flexibility with a top-tier global pharmaceutical partner. You will independently monitor Phase II–IV trials across Neurology, Rare Disease, Dermatology, and Oncology. Requires 2-3 years ...

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...

Senior Clinical Research Associate sought by ICON Plc in Madrid to lead site monitoring and trial management. This role demands expertise in GCP, regulatory compliance, and data integrity, with 60% travel. Ideal candidates possess a scientific degree, strong organizational skills, and experience ...

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...