Spécialiste de la mise en route des sites/ Site Activation Specialist
Core
Executes feasibility, site identification, regulatory, start-up, and maintenance activities for clinical research studies at the regional or country level.
Role type
Site Activation Specialist (Clinical Research)
Builds
Clinical research study sites and associated documentation
Domain
Clinical research / Life sciences
Deliverable
client delivery
Required skills
Site feasibility assessment, regulatory compliance, contract negotiation, site documentation management, performance metrics reporting, project timeline management, stakeholder coordination
Preferred skills
Knowledge of clinical trial regulations, experience with electronic data capture systems
Technologies
Internal tracking systems, databases, project management tools
Responsibilities
Serve as Single Point of Contact (SPOC) for investigative sites, prepare and verify site documentation, track execution of regulatory and ethical documents, maintain project timelines and internal systems, report on site performance metrics
Seniority
Mid-level, hands-on IC
