our client is an leading global pharma company.

1. Pre-check of returned case report forms before the data will be given in the clinical data management workflow
2. Finish data entry work
3.Operation data entry related software
4.Optimize data entry workflow and prepare related document if needed
5.Assist clinical team printing CRFS, CRF check and numbering, date entry or second person check

1.A minimum of a BA/BS degree in a health or science related field
2.A minimum of 2 years of clinical trial monitoring experience is preferred.Specific therapeutic area experience may be required depending on the position.
3. Strong working knowledge of ICH-GCP, company standard operating procedures, local laws and regulations, assigned protocols and associated protocol specific procedures including monitoring guidelines.