ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As an IHCRA at ICON, you will support the execution and management of clinical trials, contributing to the advancement of innovative treatments and therapies.
**What You Will Do:**
You will take responsibility for clinical trial monitoring deliverables, applying your skills to ensure quality and efficiency.
Key responsibilities include:
+ Assisting in the planning, initiation, and execution of clinical trial activities + Conducting site feasibility assessments and participating in site selection processes + Coordinating with investigative sites to ensure compliance with study protocols and regulatory requirements + Monitoring study ...