iconplc

Join AstraZeneca Canada as a Clinical Trial Associate in Burlington, ON. Leverage your oncology experience and clinical research expertise to coordinate trials, manage regulatory documentation, and support cross-functional teams. This hybrid role requires a Bachelor’s in a scientific field and st...

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 ...

Global Study Manager role at ICON in Canada: Lead and manage complex projects in the pharmaceutical or biotech industry. Requires a Bachelor’s degree in a scientific discipline, extensive project management experience, and strong leadership skills. Drive cross-functional teams, develop project pl...

Senior Local Trial Manager – Oncology role in Blue Bell, US. Requires BA/BS in health/science, 3–5+ years end-to-end trial management, and solid tumor oncology experience. You’ll ensure top-quality country-level trial delivery, manage vendors, and drive inspection readiness. Benefits include annu...

Join ICON as a Medical Data Reviewer in Blue Bell, PA. Leverage your MD, MBBS, or PharmD to ensure clinical trial data accuracy and safety. Collaborate with global teams on medical review, GCP compliance, and safety signal detection. Enjoy competitive benefits including health insurance, retireme...

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 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 in Dublin as a Clinical Python Developer to drive data-driven decisions in clinical trials. Leverage 4+ years of Python, PySpark, and Spotfire expertise within CDISC-guided environments. Transform complex clinical data into insights using modern tech stacks and Databricks. Enjoy ben...

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...