We're sorry, the job you are looking for at IQVIA on EuroPharmaJobs has expired.
Click here to see more jobs at IQVIA .
We still have many live jobs. Click below for similar jobs in:
or go to our job search page.
In this role, you will provide expert support for clinical trial quality, ensure compliance with ICH-GCP and global regulatory expectations, and act as a key partner to internal teams and CROs. You will be responsible for quality oversight, process
The candidate will serve as the bioanalytical expert for LC-MS and oversees outsourced LC-MS-based assay development, validation and sample analysis by bioanalytical vendors in support of regulated nonclinical and clinical studies for several of the