Description
The Site Navigator II coordinates site-level activities during the start-up and potentially closeout phases of clinical studies, serving as the primary contact for investigative sites. The role manages site selection, feasibility, outreach, regulatory and IRB/IEC submissions, site activation, document and TMF compliance, supply coordination, contract and budget negotiations, protocol and CRF review, data validation, and site monitoring. It requires remote-based work with possible office presence, limited training travel, and strong clinical research, ICH/GCP, and regulatory knowledge.
