Experienced Clinical Research Associate Sponsor-dedicated

Job description

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. The role involves conducting site monitoring visits, working with sites to adapt and track subject recruitment plans, administering protocol and related study training, and evaluating the quality and integrity of study site practices

Requirements

• Excel
• Word
• PowerPoint
• English language
• effective communication
• knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

Skills