Job Description

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

You will be responsible for:

• Being the main point of contact between site personnel and CRA involved in the project helping on query resolution and EDC completion.
• Serving as the primary sites’ contact point for vendors, study supplies, and access management.
• Ensuring that pre-study testing (scans, MRI/CT qualification questionnaires, test ECGs, etc.) of local site facilities is completed.
• Assisting the Monitors in their prompt completion of all subject event and site event information in CTMS; tracking the resolution status of site issues and action items in CTMS.
• Acting as the one who will ensure the order, receipt, inventory storage, distribution, return/recall, and reconciliation of clinical supplies.
• Ensuring regulatory an...