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Docs Global (Continental Europe) – Madrid – This is an exciting opportunity for motivated, experienced SCRA to join one of the world’s largest providers of functional service solutions to the pharmaceutical industry and make a significant contribution to the development of new medicines that will have a real benefit for patients around the world. Requirements: Roles & Responsibilities of the position Role and Responsibilities: – A Clinical Research Associate, is the person in Trial Co-ordination and Site Management that serves as primary contact point between the sponsor and the investigational site. – A Clinical Research Associate, is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company’s Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. – Responsibilities include site selection, pre trial assessment, subject recruitment and retention planning, site initi…