Found Description
Overview
Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents and information. CVs in English only.
Responsibilities
- Be the main point of contact between site personnel and CRA involved in the project, assisting with query resolution and EDC completion.
- Serve as the primary site contact 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.
- Assist Monitors in the prompt completion of all subject event and site event information in CTMS.
- Track the resolution status of site issues and action items in CTMS.
- Ensure the order, receipt, inventory storage, distribution, return/recall and reconciliation of clinical supplies.
- Ensure regulatory and ethics committee...