10 ago - Italia
Opis
OPIS S.r.l. is seeking a Clinical Research Associate to manage and monitor clinical trials in compliance with study protocols, ICH-GCP and applicable regulations.
The role includes site selection, initiation, monitoring and close-out activities, while ensuring data quality and patient safety. The successful candidate will conduct feasibility, pre-study, initiation, monitoring visits, perform SDV, monitor recruitment, and support sites to meet targets.
J-18808-Ljbffr
29 ago - Roma
gej service srls
29 ago - Rimini
Phoenix Nexus
29 ago - Lecce
Fugu
29 ago - Bari
Siemens