Clinical Trial Coordinator
IQVIA H · Shanghai, China · listed 7 days ago
Clinical Research
Responsibilities include, but are not limited to: • Trial and site administration: o Track (e.g. essential documents) and report o Ensure collation and distribution of study tools and documents • Document management: o Prepare documents and correspondence o Collate, distribute/ship, and archive…
Read the full description
Free registration — your contact details plus five quick fields about the role you want, or your CV — unlocks every description on the site, plus the apply link.
- The complete posting, as the employer wrote it
- Apply directly on IQVIA H's own site
- A match score on every job, from your profile or your CV