Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information.

Responsibilities

• Being the main point of contact between site personnel and CRA involved in the project, helping on query resolution and EDC completion.
• Serves as the primary site’s contact point for vendors, study supplies, and access management.
• Ensure that pre‑study testing (scans, MRI/CT qualification questionnaires, test ECGs, etc.) of local site facilities is completed.
• Act as the one who will ensure the order, receipt, inventory storage, distribution, return/recall and reconciliation of clinical supplies.
• Ensures regulatory and ethics committee submissions and notifications, staying up to date on local regulations and dispositions.
• Coordinate preparation for and follow‑up on site, TMF and systems audits and inspections.
• Manage the TMF...