Nuestros clientes
Pharmaceutical services company that provides integral solutions for the pharmaceutical industry with a full CRO service therapeutically focused on oncology, endocrinology and internal medicine. The company provides CRO services mainly in phases I to IV of research.

Descripción de la oferta
Reporting to the Project Manager in charge of the Trial you will perform clinical monitoring activities in compliance with ICH GCP and Regulatory requirements.

You will be in charge of overseeing clinical trials and compliance with regulatory requirements for phase I to IV studies, working with diverse hospital teams. You will have to conduct monitoring visits, to obtain details of existing regulations and hospitals requirements. You will report all visits and contacts with Investigators in writing to Project Manager. You will ensure full traceability of all essential documents. You will provide ongoing support to Investigators and study site personnel during the study.

Qué buscamos
-Ideal candidates will provide an University degree in life sciences (pharmacy, biology) with at least one year experience in study monitoring. Fluency in Spanish and English (written and spoken) is a must.

-We are looking for people with excellent communication skills and computer literacy, with current driving licence and availability to travel.
 

Qué ofrecemos
Career development with a training plan and a flexible timetable.