Bio-Rad Labs Clinical Trials Specialist SH in Shanghai, China
10% Identify qualified clinical sites in certain region
10% Get the EC approval form clinical sites
15% Prepare initiation meeting, middle stage meeting and close meeting of each clinical site in certain
10% Guarantee the qualified patients/samples recruitment in required time in each clinical site in certain
10% Regular visit to the clinical sites in certain region
10% Work out audit plan to the clinical sites which are operated by other colleagues
15% Conduct audits based on the audit plan
10% Work out audit summary and record
5% Guarantee all the documents/record are archived and meet the regulatory requirements.
5% Quality control process improvement of clinical trials.
Tracking Code: 11059-446
Job Location: Shanghai, , China
Position Type: Full-Time/Regular