Responsibilities (a) Site management - Study site selection, initiation (SIV) and clinical monitoring.
- Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience.
- 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.
- Ensure Principal Investigator/study staff complies with safety reporting requirements, as defined in protocol, SOP, ICH-GCP and GCP.
- Track study recruitment to ensure recruitment target is achieved in all studies.
- Conduct monitoring visit according to SDV plan and SOP;

address issues with sites and complete monitoring visit report in a timely manner coordinating.
- Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study.
- Assemble site specific EC submission dossier, and ensure submission to EC.



Training - Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements.
- Conduct site initiation to ensure that the site has a thorough understanding of the study protocol and requirements. Documentation - Ensure timely collection of essential documents in compliance with protocol and regulations at study start-up, during and at study close-down. Maintain and update these documents in investigator files, trial master files.
- Prepare/complete study records’ archiving according to protocol and sponsor requirements. (b) Drug Safety - Ensure safety information is disseminated to all sites according SOP and applicable regulations.
- Ensure SAE is reported within the timeline in compliance with SOPs and applicable regulations. (c) Finance and Administration - Finalize budget and obtain signed contract from site, prior to site initiation visit.
- Ensure Study

📌 Contractor Cra_spain (Sabiñánigo)
🏢 Tigermed
📍 Sabiñánigo