Site Activation Specialist, ICF Lead
Core
Country-level Site Activation (SA) activities ensuring compliance with local regulations, SOPs, and project requirements for clinical studies.
Role type
Senior individual contributor Site Activation Specialist
Builds
Study start-up deliverables and site activation pipelines
Domain
Clinical research / Life Sciences
Required skills
Feasibility assessments, site identification, regulatory submissions, document review, quality control, project planning, stakeholder collaboration
Preferred skills
Local regulatory expertise, cross-functional management, process improvement
Technologies
Internal systems, databases, tracking tools
Responsibilities
Act as Single Point of Contact for assigned studies; Perform feasibility assessments and site identification; Prepare and review site documentation (CDAs, SIFs, ICFs, IPs); Maintain accurate data in internal systems; Review site performance metrics; Align on project plans and timelines; Provide local regulatory expertise to project teams.
Seniority
Senior, hands-on IC
