Experienced Clinical Research Associate, France Based
IQVIA UK
France
Not specified (further details needed)
Good clinical practice (gcp) knowledge
International conference on harmonization (ich) guidelines
Site monitoring visit execution
IQVIA UK is seeking an Experienced Clinical Research Associate based in France to perform site monitoring and management in accordance with regulatory requirements. The role involves ensuring compliance with study protocols, managing site relationships, and facilitating effective project execution
Job Summary
The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with GCP and ICH guidelines.
Candidates will be responsible for evaluating the quality of study site practices and managing the progress of assigned studies through data tracking and query resolution.
The position requires maintaining accurate documentation in the Trial Master File and ensuring Investigator's Site Files comply with local regulatory requirements.
Matching Summary
Match Score: 85
IQVIA UK is seeking an Experienced Clinical Research Associate based in France to perform site monitoring and management in accordance with regulatory requirements. The role involves ensuring compliance with study protocols, managing site relationships, and facilitating effective project execution.
Skills & Requirements
Must-have
Good Clinical Practice (GCP) knowledge
International Conference on Harmonization (ICH) guidelines
Site monitoring visit execution
Subject recruitment plan management
Trial Master File (TMF) maintenance
Nice-to-have
Strong problem-solving skills
Effective time management abilities
Financial management experience
Collaborative team player mindset
Key Requirements
At least 1 year of on-site monitoring experience
High School Diploma or equivalent Degree in scientific discipline
Proficiency in Microsoft Word, Excel, and PowerPoint