in a scientific discipline.
• Experience: 1-4 years of experience in site monitoring within clinical research.
• Skills: Strong understanding of ICH GCP and applicable clinical trial regulations; excellent verbal and written communication; ability to multitask...
Oversight: Assist in overseeing the manufacturing processes of viral vectors, ensuring that the production is compliant with relevant EU and US regulations. Monitor and support the analytical control of materials intended for clinical trials, ensuring...
Oversight: Assist in overseeing the manufacturing processes of viral vectors, ensuring that the production is compliant with relevant EU and US regulations. Monitor and support the analytical control of materials intended for clinical trials, ensuring...
Lavoro Clinical Monitor a Frosinone – Offerte simili: