Opportunity Description
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...
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