Senior CRA: Global Site Monitoring & Compliance Lead

Parexel is looking for a Senior Clinical Research Associate to manage site monitoring and ensure the quality execution of clinical trials. Responsibilities include overseeing site management, maintaining investigator relationships, and ensuring compliance with Good Clinical Practices (GCP). The ideal candidate will have a minimum of 3 years of relevant monitoring experience, preferably in Oncology. A Bachelor’s degree in life sciences is required, along with effective communication skills and a valid driver’s license. Travel (60-80%) is expected.
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