**Clinical Study Administrator**:
**Location: CDMX**
**Hybrid work - 3 office days**
- Interfaces with Investigators, external service providers and CRAs during the document collection process to support effective delivery of a study and its documents.
- Operational responsibility for the correct set-up and maintenance of the local eTMF and ISF including document tracking in accordance with ICH-GCP and local requirements.
- Ensures essential documents under their responsibility are uploaded in a timely manner to maintain the eTMF "Inspection Readiness".
- Ensures that all study documents are ready for final archiving and completion of local part of the eTMF and supports the CRA in the close out activities for the ISF.
- Coordinates administrative tasks during the study process,



audits and regulatory inspections, according to company policies and SOPs.
- Leads the practical arrangements and contributes to the preparation of internal and external meetings e.g., study team meetings, Monitors' meetings, Investigators' meetings.
Liaises with internal and external participants and/or vendors, in line with international and local codes.
- Prepares, contributes to and distributes presentation material for meetings, newsletters and websites.
**Essential Skills**
- Bachelore degree
- English - Basic/Intermediate
- Excel - Intermediate/advanced

📌 Clinical Study Administrator (San Luis Potosí)
🏢 Astrazeneca
📍 San Luis Potosí