C

Manager, Regulatory Clinical Trial Authorization (CTA)

CSL·Glattbrugg·13.05.2026

 csl.wd1.myworkdayjobs.com

 
full_time80–100%

 

This role manages clinical trial authorizations. Daily tasks include planning and overseeing CTA activities. Requirements include strong regulatory knowledge. Nice-to-haves are experience with quality standards and audit preparation. The role offers growth in regulatory affairs. Notable perks include a focus on quality and inspection readiness.