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 sites in accordance with regulations and SOPs.
Role type
Site Activation Specialist (Clinical Research)
Builds
Site activation and maintenance for clinical research studies
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Site documentation management, contract negotiation, regulatory compliance, project timeline management, performance metrics reporting, Single Point of Contact (SPOC) coordination
Preferred skills
Knowledge of clinical research regulations, experience with Investigator Pack (IP) and Informed Consent Forms (ICF)
Responsibilities
Prepare and manage site documentation; review and negotiate site documents and contracts with sites and sponsors; track completion of required documents (CDAs, ethics, ICF); update internal systems and project plans; serve as primary point of contact for investigative sites.
Seniority
Mid-level, hands-on IC
