Partenaire d'Activation de Site I / Site Activation Partner I

Job Overview

The Site Activation Partner I (Sr Associate) is responsible for leading or supporting operational activities from start‑up to close‑out for assigned studies and investigator sites. The role ensures compliance with study and country deliverables, timelines and quality standards in accordance with prevailing laws, Good Clinical Practices (GCP) and Pfizer standards.

Responsibilities

• Site Activation Responsibilities:
  • Initiate and coordinate activities for compiling Investigator Initiation Packages.
  • Manage regulatory submissions and collaborate with global and local regulatory groups.
  • Support site activation to meet timelines and quality standards.
• Clinical Trial Conduct:
  • Update documents such as protocol amendments, ethics committee approvals and regulatory activities throughout the study lifecycle.
  • Ensure accurate filing and system updates to track site compliance...