OPIS is seeking a Clinical Data Manager to support planning, execution, and delivery of data management activities across clinical trials and investigations. Responsibilities include creating and maintaining CDMPs, CRFs, and data transfer specs, and ensuring regulatory compliance.
The role requires a Bachelor's degree and at least 2 years in a similar CRO/pharma setting, with solid English communication and proficiency in Microsoft Office.
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📌 Clinical Data Manager: CDISC & Trial Data Lead (New South Wales)
🏢 opissrl
📍 New South Wales
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