Senior Clinical Research Associates

Roles and Responsibilities
To maintain awareness of local regulatory requirements, and to conduct studies in accordance with SOPs, guidelines and ICH Good Clinical Practice guidelines
To provide assistance, where directed by the Project Manager, in specific tasks relating to the preparation of national and international projects
Co-ordination of CRAs and individual steps of national or multinational multicentre trials
Quality Control of monitoring functions and supervision of GCP compliance as well as time lines
Preparation and implementation of project meetings and investigators’ meetings
Training on the job for new CRAs and Project Assistants
Requirements
At least 2.5 Yrs of established experience as a CRA
Study of natural science (biology, chemistry), medicine, pharmacy or qualification as medical documentalist, health care specialist, paramedic professional
Excellent command of native language
Good command of written and spoken English
Willingness to travel extensively
The ability of a good communication, dedication, reliability and a talent for organising are required
Excellent organisational skills and team leading skills
Location