Senior Study Start Up Associate (Regulatory Submissions)

Senior Site Partner

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.

We are currently seeking a Site Partner to join our diverse and dynamic team. As a Site Partner at ICON, you will independently manage relationships with a portfolio of investigator sites, supporting their engagement and performance across studies. You will act as a trusted liaison, advocating for site needs internally while supporting ICON processes and expectations.

What You Will Be Doing:

• Preparation and supply of site documentation required for regulatory submissions CEP/CONEP. in CROs

• Ensure timely ethics submission of protocol and study documents/safety reports for local ethics/IRB approval according to local requirements.
•...