iconplc - United Kingdom, Reading, IT - Administration

Seeking a Senior Clinical Trial Associate in Reading or Cambridge, UK. Leverage your clinical trial support expertise and regulatory knowledge to manage documentation, coordinate meetings, and ensure compliance. Requires a Bachelor's in a scientific field, strong organizational skills, and profic...

Senior Clinical Supplies Project Manager sought by ICON plc, a world-leading clinical research organization. This role manages global pharmaceutical supply and CMC activities across all development phases. Ideal candidates bring 3-4 years of clinical supply project management experience. Enjoy fl...

Seeking a detail-oriented **Project Manager, IRT** in **Reading, UK** to lead system activities from award to closeout. Leverage 4+ years of PM experience and clinical research expertise to drive timelines, budgets, and stakeholder communication. Enjoy benefits like annual leave, health insurance...

Join ICON plc as a Clinical Research Associate II in Reading. You will conduct site monitoring visits, ensure ICH-GCP compliance, and contribute to innovative clinical trials. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We offer competitive benefit...

Join ICON plc in Reading as a Senior Clinical Supplies Project Manager. Lead clinical supply projects, ensuring timely delivery for global trials. Utilize your 5+ years of supply chain experience to optimize processes and ensure regulatory compliance. Enjoy competitive benefits while shaping the ...