a) Site management - Study site selection, initiation (SIV) and clinical monitoring.

- 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.
- c) Finance and Administration - Finalize budget and obtain signed contract from site, prior to site initiation visit.
- Qualifications 3.1 Bachelor degree or above in Medical, Pharmacology or Biology related major. 3.2 At least 8 year of CRA experience; 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 (Galicia)
🏢 Tigermed
📍 Galicia