Act as PAREXEL’s direct contact with assigned sites
Assess and ensure overall integrity of study implementation and adherence to study protocol at clinical sites
Build relationships with investigators and site staff
Facilitate and support site with access to relevant study systems and ensure sites are compliant with project specific training requirements
Identify and evaluate potential data quality and data integrity issues and determine and implement appropriate follow-up action
Monitor and maintain compliance with ICH-GCP and applicable international and local regulations
Ensure timely and accurate completion of project goals and update of applicable trial management systems

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

Clinical Research Associate II

Key skills