Site Activation Specialist
Core
Execute site activation activities for clinical research studies in Argentina, serving as the Single Point of Contact for investigative sites and managing regulatory document preparation and tracking.
Role type
Site Activation Specialist (Clinical Research)
Builds
Clinical trial sites ready for patient enrollment
Domain
Clinical Research / Life Sciences
Deliverable
physical/clinical work
Required skills
Clinical research regulatory activities, Ethics committee presentations, ANMAT (SSU and maintenance phases), Site activation procedures, Regulatory document preparation, Internal system/database management, Project timeline planning, Quality control of site documents
Preferred skills
Clinical trial assistant experience, Direct contact with sponsors
Technologies
Internal systems, databases, tracking tools
Responsibilities
Serve as Single Point of Contact for assigned studies; Perform start up and site activation activities; Prepare and review site regulatory documents for completeness and accuracy; Track and follow up on the approval and execution of regulatory, ethics, and Investigator Pack documents; Provide local expertise to Site Activation Managers and project teams; Perform quality control of documents provided by sites.
Seniority
Mid-level, hands-on IC
