Job Description
Parexel in Australia is seeking a Site Activation Specialist to drive regulatory and site activation activities across clinical trials.
You will coordinate documents, liaise with investigators, ethics committees, and client study teams to ensure timely initiation and ongoing trial support.
Key responsibilities include managing regulatory submissions, maintaining TMF, and supporting site audits.
The role emphasizes collaboration, accuracy, and adherence to GCP and Parexel standards in a global
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📌 Global Site Activation Coordinator (New South Wales)
🏢 Parexel
📍 New South Wales
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