Sr Site Activation Coordinator
Core
Execute feasibility, site activation, and maintenance activities for investigative sites in clinical studies, ensuring document completeness and regulatory compliance.
Role type
Senior individual contributor site activation coordinator
Builds
Clinical study sites and associated regulatory documentation
Domain
Life sciences / Clinical research
Required skills
Site activation, feasibility studies, document review, regulatory compliance, SOP adherence, database management, stakeholder coordination
Preferred skills
Experience with Investigator Pack (IP) release, Informed Consent Form (ICF) management, Contractual Document Agreement (CDA) tracking
Technologies
Internal tracking tools, project management systems, databases
Responsibilities
Perform feasibility and site activation tasks for assigned studies; prepare and review site documents for accuracy; track and follow up on regulatory and ethics document approvals; update internal systems and project plans; distribute completed documents to sites and internal teams.
Seniority
Senior, hands-on IC
