The main role is to contribute to ensure the compliance of clinical trials conducted in China.
In collaboration with clinical operations organization in China, be responsible for establishing, maintaining and continually improving the clinical quality system; review of quality system documentation, conduct GCP audits, training, deviation handling, inspection readiness etc.
Ensure the implementation of global clinical processes at local level
While necessary, support the GCP audts in Pan Asia .
What you'll need to succeed
What you'll get in return
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career. #1234184
19 Jan 2023
Talk to a consultant
Talk to Lennie Wang, the specialist consultant managing this position, located in Shanghai
Unit 1205-1212, HKRI Centre One, HKRI Taikoo Hui, 288 Shimen Road (No.1)