Clinical Trial Admin & Documentation Specialist (New South Wales)

Clinical Trial Admin & Documentation Specialist (New South Wales)

21 Sep
|
Iqvia
|
New South Wales

21 Sep

Iqvia

New South Wales

Job Description

IQVIA in North Sydney, NSW is seeking a full time TMF Administrative Support to assist CRAs and RSU teams in maintaining Trial Master File documents, tracking site compliance, and ensuring timely TMF delivery.

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You will help prepare, file, archive clinical documents, manage CRF tracking, and support on-site visits as needed. Requires a high school diploma, 3 years of admin experience, and proficiency in Word, Excel and PowerPoint; good English communication and organizational skills.

📌 Clinical Trial Admin & Documentation Specialist (New South Wales)
🏢 Iqvia
📍 New South Wales

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