Site Documents Jobs in Beijing
-
Job Type
-
Posting Date
7 Jobs Found | Sort By : Relevance | Posted Date
Less results matching your search!
Try removing some of the filters to get more results
No results matching your search!
Try removing some of the filters to get more results
Fsp Cra Ii (beijingharbinchangchun)
Fortrea
Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...
Ssu Site Manager
Iqvia
Under general supervision serve as Single Point of Contact (SPOC) in assigned studies for investigative sites Site Activation Manager (SAM) Project Management team and other departments as necessary. Ensure adherence to standard operating procedures (SOPs) Work Instructions (WIs) quality of designa...
Fso Cra Ii (beijing)
Fortrea
Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...
Fso Cra Ii (beijingtianjin)
Fortrea
Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...
Fsp Cra Iizhengzhou
Fortrea
Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...
Fsp Cra Ii (beijing)
Fortrea
Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...
Spclst, Clin. Operations
Msd R&d
Job DescriptionThe CTA is an administrative support role for clinical trials. The role responsibilities include but not limited to the following activities:Basically Safety reports distribution and tracking. TMF support for country level document uploading to eTMF assist with eTMF reconciliation CDA...