Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and relevant regulations.

- Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating.
- Training
- Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements.
- Finalize budget and obtain signed contract from site, prior to site initiation visit. xugodme
- 3.1 Bachelor degree or above in Medical, Pharmacology or Biology related major.

3.2 At least 8 year of CRA experience;

Cualquier información adicional que necesite para este trabajo se encuentra en el texto a continuación. Asegúrese de leerla detenidamente y luego envíe su solicitud.

3.3 Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/procedures;

3.4 Good skills on Microsoft Word, Excel, PPT and Outlook, etc.

📌 Contractor CRA_Spain (Foz)
🏢 Tigermed
📍 Foz