Clinical Research Associate, Sponsor Dedicated

To be eligible for this position, you must reside in the same country where the job is located.

Seeking _experienced_ candidates near **major hub airports in the Southeast, Northeast, Central and West regions.**

**Job Overview**
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. **Position requires 65-70% nationwide travel.**

**Essential Functions**
• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.
• Administer protocol and related study training to...