You will be responsible for scientific input to clinical development strategies and therapeutic areas.
Provide scientific and clinical development input for the safe and efficient execution of assigned programs, ensuring the highest quality and full compliance of all outputs.
Will contribute to the development of the scientific strategy of the clinical development plan, the design of trial related documents and the scientific oversight of clinical trials.
You will facilitate a team to define and deliver the clinical strategy within programs.
Define scientific strategy for multiple program components.
You will lead the development of Clinical Development Program.
Author clinical study documents and assists with development/critical review of submission documents.
Contribute to authorship and review of manuscripts and conference abstracts.
Collaboratively develop the clinical deve...
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