Principal Clinical Research Associate
About this role
Job title: Principal Clinical Research Associate
What You Will Do
Your focus will be on coordinating clinical trial monitoring delivery, resolving issues, and developing team capability.
Key responsibilities include:
- Leading site management activities, including site selection, initiation, monitoring, and close-out visits, to ensure compliance with study protocols and regulatory guidelines.
- Serving as the primary point of contact for clinical sites, addressing site queries, and resolving issues to maintain site engagement and performance.
- Ensuring the integrity of clinical data by conducting thorough source data verification, reviewing site records, and monitoring for protocol deviations.
- Mentoring and providing guidance to CRAs, contributing to their professional development and supporting the consistent application of best practices across studies.
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