Parexel
A leading global clinical research organization is seeking a Senior Clinical Research Associate to manage site monitoring and ensure the quality of clinical trials. You will be responsible for overseeing investigator site relationships, compliance with Good Clinical Practices, and conducting on-site monitoring to ensure patient safety. Ideal candidates should have a bachelor’s degree in life sciences and at least three years of monitoring experience, preferably in oncology. Travel requirements are substantial, emphasizing flexibility and adaptability.
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