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Fsp Cra Ii (beijingharbinchangchun)

Fortrea

profile Beijing - China

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...

Posted 1 week ago
Full Time

Ssu Site Manager

Iqvia

profile Beijing - China

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...

Posted on 16 Oct
Full Time

Fso Cra Ii (beijing)

Fortrea

profile Beijing - China

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...

Posted on 09 Oct
Full Time

Fso Cra Ii (beijingtianjin)

Fortrea

profile Beijing - China

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...

Posted on 09 Oct
Full Time

Fsp Cra Iizhengzhou

Fortrea

profile Beijing - China

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...

Posted on 30 Sep
Full Time

Fsp Cra Ii (beijing)

Fortrea

profile Beijing - China

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...

Posted on 19 Sep
Full Time

Spclst, Clin. Operations

Msd R&d

profile Beijing - China

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...

Posted on 14 Sep
Full Time