Senior Clinical Research Associate: Site Monitoring Lead

Parexel seeks a Senior Clinical Research Associate in Montpelier, Vermont to manage and monitor clinical trial investigator sites. The role requires a minimum of 3 years of monitoring experience, particularly in Oncology, and ensures the safety and quality of clinical trials while adhering to regulatory standards. Responsibilities include site management, oversight of trial conduct, and effective communication with study teams and investigator sites. Applicants must hold a degree in life sciences and possess strong knowledge of clinical methodologies.
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