Clinical Research Associate - Sponsor Dedicated - Bilingual

Job Description

The Clinical Research Associate is responsible for site qualification, initiation, monitoring, management, and close-out visits, ensuring compliance with regulatory guidelines. They also assess site performance, manage site-level activities, and support subject recruitment and retention strategies.

Requirements: Candidates should have a strong understanding of ICH/GCP guidelines and relevant regulations. Experience in clinical research and site management is preferred, along with the ability to adapt to changing priorities.

Key Skills: Clinical Research, Site Management, Regulatory Compliance, GCP, Data Integrity, Patient Safety, Monitoring, Documentation, Query Resolution, Training, Collaboration, Problem Solving, Communication, Project Management, Data Collection, Audit Readiness