Support study planning, preparation and initiation (e.g. set study time plans/milestones, obtain ethics and regulatory approvals, import study products, communicate the central laboratory and logistic arrangements, and organize study initiation meetings);
Monitor the progress and quality of study activities (both on-site at study centres and off-site via online electronic systems);
Oversee study centres’ compliance with study protocols, Good Clinical Practice (GCP) and other research ethics and regulatory requirements, and write monitoring reports;
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Drive the transformation and simplification of Advisory processes through a customer journey lens, leveraging digitalization while maintaining a strong governance and control foundation.
Collaborate closely with complaints and surveillance teams to leverage case learnings, continuously strengthen existing governance frameworks, enhance controls, and drive ongoing improvement in the risk and control environment.
More than 3 years of experience in related or front office advisory roles
...
Drive the transformation and simplification of Advisory processes through a customer journey lens, leveraging digitalization while maintaining a strong governance and control foundation.
Collaborate closely with complaints and surveillance teams to leverage case learnings, continuously strengthen existing governance frameworks, enhance controls, and drive ongoing improvement in the risk and control environment.
More than 3 years of experience in related or front office advisory roles
...