CSL''s RandD organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we''re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. The incumbent will be responsible for the quality and delivery of high-quality clinical development documents and oversight of clinical study delivery across the portfolio in collaboration with strategic CRO partners. Responsible for overseeing the recruiting, staffing and development of the clinical scientists and medical writing specialists in the group. Serve as the decision support lead for the SVP Portfolio Development (PD) and ensure excellence throughout the Portfolio Development organization. Oversight of Individuals Recruiting, staffing, training and development of clinical scientists and medical writing specialists in the group, to maintain a dynamic and cutting-edge level of medical scientific expertise and advanced drug development approaches Ensuring delivery of high-quality clinical development content including: Clinical development plans, protocols, study reports, common technical document modules and publications in academic journals Regulatory submissions and meetings Stage-gate and benefit -risk evaluations and assessments Presentations at scientific and technical review committees Implemen