Senior Clinical Trials Lead: Site Management & Compliance

Parexel is seeking an experienced Clinical Research Associate to support investigator/site selection, monitoring activities, and regulatory start-up tasks. You will train site staff, ensure training is documented, and maintain inspection readiness across multiple sites.

Your role includes on-going monitoring (remote and on-site), SDR/CRF review, data verification, and QA compliance, with regular collaboration with LSAD, CQAD and MSLs. Travel will be required.

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