Clinical Trial Coordinator I

**Work Schedule**

Standard (Mon-Fri)

**Environmental Conditions**

Office

**Job Description**

**Job-related skills**

+ Excellent technical/IT skills. Able to understand the impact of technology on studies and
+ to use and develop computer skills while making appropriate use of client systems/software.
+ Knowledge of ICH GCP relevant operational procedures, systems, and quality guidelines
+ regarding clinical studies
+ Able to work independently as well as in a team.
+ Professional attitude with good customer focus (internal and external)
+ Time Management as safety notifications, eTMF etc. need to be done in a timely manner.

**Job Responsibilities**

+ Maintain up to date participating center’s information (including all contact details).
+ Responsible for preparing the Investigator and Sponsor files (electronic and/or paper) with essential documents for the initiation of sites participating in c...