CSLs R&D 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
Overview: The Manager, Clinical Trial Authorization (CTA) is responsible for ensuring that CTA activities for assigned clinical studies are planned, governed, and overseen in line with CSL regulatory expectations, quality standards, and development timelines. Reporting to the
The Senior Statistical Programmer is responsible for providing hands-on support and technical guidance on clinical study teams. The development of study and ad hoc output, including, but not limited to: ADaM datasets, tables, figures, and listings output
Analytical Measurements: You perform routine sample measurements using a variety of analytical techniques, including but not limited to porosimetry measurements (BET, mercury intrusion), elemental analysis, and titration methods. Instrument Calibration & Validation: You calibrate analytical equipment
Analytical Measurements: You perform routine sample measurements using a variety of analytical techniques, including but not limited to porosimetry measurements (BET, mercury intrusion), elemental analysis, and titration methods. Instrument Calibration & Validation: You calibrate analytical equipment