As a Project Manager – Feasibility & Site Activation, you will play a critical role in driving the successful start-up of global clinical studies
Job Summary
As a Project Manager – Feasibility & Site Activation, you will play a critical role in driving the successful start-up of global clinical studies.
You will work at the center of cross-functional collaboration, partnering with sponsors, internal teams, and sites worldwide to deliver start-up excellence at scale.
In addition to your competitive salary, ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.
Matching Summary
As a Project Manager – Feasibility & Site Activation, you will play a critical role in driving the successful start-up of global clinical studies.
Skills & Requirements
Must-have
Study Start-Up strategy and execution
global, multi-country studies
regulatory and ethics submissions
site contract and budget negotiations
ICH-GCP and applicable regulatory frameworks
Nice-to-have
foster an inclusive environment
driving innovation and excellence
continuous improvement across regions
culture of performance, collaboration, and accountability
Key Requirements
Proven experience managing Study Start-Up (SSU)
Experience working on global or multi-country clinical studies
Strong knowledge of regulatory and ethics submission processes
Experience coordinating site contracts and budgets
Familiarity with CTMS, eTMF, and clinical trial systems