Архив: Clinical Research Associate. Москва.

Описание

Responsibility: To maintain awareness of local regulatory requirements, and to conduct studies in accordance with SOPs, guidelines and ICH Good Clinical Practice guidelines Conduct as well as pre-/Post-processing of pre-study-, initiation-, monitoring- and close out-visits Creating study relevant documents Communication with investigational sites Participation in national/international project and investigational meetings Regula business trips

Requirements:

Medical or pharmaceutical high education 3+ years experience in the monitoring of clinical trials To be able to manage multiple tasks and achieve deadlines on time Self-organized To be ready for travel Emotionally stable Good knowledge of English

We offer:

Office or home based

График

Полная занятость, полный день

Компания

Экрон акунова

Опыт работы

3–6 лет

Город

Москва

Категория

Медицина и фармацевтика