Clinical Research Associate

Telecommute · Paris, Île-de-France, France · Clinical Monitoring

Description

The Clinical Research Associate (CRA) is part of Clinical Monitoring within TFS Develop and will function operationally as a member of a Project Team and is responsible for the initiation, on–site and remote monitoring and termination of investigative sites during study conduct, according to company policies, SOPs and regulatory requirements.

The CRA may conduct all stages of site monitoring (feasibility, pre-study, initiation, interim, and close-out). Ability to travel as needed: may involve overnight and international travel.

ESSENTIAL JOB FUNCTIONS

Requirements

MINIMUM REQUIREMENTS


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