Sr Site Activation Specialist
Core
Execute country-level Site Activation activities for clinical research studies, ensuring regulatory compliance and document accuracy for investigative sites.
Role type
Senior individual contributor Site Activation Specialist
Builds
Clinical research study sites and activation documentation
Domain
Life sciences / Clinical research
Required skills
Clinical research experience, Site activation, Regulatory compliance, Document management, Project planning, Quality control, Stakeholder communication, Data entry, Feasibility assessment, Site identification
Preferred skills
Leadership experience, Systems enhancement, Contingency planning
Technologies
Internal systems, databases, tracking tools, Investigator Pack (IP), Informed Consent Form (ICF), CDA/SIF
Responsibilities
Serve as Single Point of Contact for assigned studies; Perform feasibility, site ID, start up, and activation activities; Prepare and review site documents for completeness and accuracy; Maintain internal systems and databases; Review and track document execution progress; Provide local expertise to project teams; Perform quality control of site-provided documents.
Seniority
Senior, hands-on IC
