Medical Data Manager for Clinical Trials

1 week ago


Auckland, Auckland, New Zealand George Clinical Pty Full time
About the Role

In this role, you will provide medical oversight for clinical trials, ensuring patient safety and adherence to protocol. You will serve as the primary medical contact for study teams, investigators, and sponsors.

You will be responsible for reviewing and assessing adverse events, serious adverse events (SAEs), and safety reports. Additionally, you will contribute to protocol development, study design, and medical monitoring plans.

This position requires strong communication and collaboration skills to work effectively with global teams. A Medical Doctor (MD) qualification is required, and at least 5 years of experience as a Medical Monitor in clinical trials is preferred.



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