24 Sep
|
Novotech
|
Sydney
Novotech seeks a Consultant within DDC to provide regulatory and product development support to stakeholders, manage client projects, and facilitate progression through clinical trials. You will draft regulatory documents, liaise with regulatory authorities (TGA, OGTR, NZ EPA), and develop regulatory strategies across jurisdictions.
The role requires 3+ years in Australian regulatory affairs, a life sciences degree, solid English, and proven ability to manage multiple milestones in a fast-paced
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📌 Regulatory Affairs Consultant - Clinical Trials (Australia) (Sydney)
🏢 Novotech
📍 Sydney