CRA – Italy – Oncology, Rare Disease

Responsible for site qualification, initiation, interim monitoring, site management and study close-out visits for studies in accordance with Good Clinical Practices (GCPs) and applicable local and international regulations and Standard Operating Procedures (SOPs). Ensure quality of data submitted from study sites and assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.

Link: https://worldwide.gr8people.com/jobs/2762/cra-italy-oncology-rare-disease

Accedi

Cerca sul sito