About this role

Act as Parexel’s direct contact with assigned sites
Assess and ensure overall integrity of study implementation and adherence to study protocol
Build relationships with investigators and site staff
Facilitate and support site with access to relevant study systems
Evaluate site recruitment plan in collaboration with the site staff on an ongoing basis and provide strategy for improvements
Conduct remote visits/contacts as requested/needed
Ensure timely and accurate completion of project goals and update applicable trial management systems
Monitor and maintain compliance with ICH-GCP and applicable international and local regulations

Site Management experience or equivalent experience in clinical research
Understanding of clinical trials methodology and terminology
Educated to degree level (biological science, pharmacy, or other health-related discipline preferred) or equivalent nursing qualification or other equivalent experience
Knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS), and MS-Office products such as Excel and Word

Clinical Research Associate – FSP

Key skills