上海招聘

CRA Job Description：

1)      Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation;

2)      Coordinating the clinical trial conduction in whole process by following GCP, SOP and Protocol strictly;

3)      Coordinating and giving input to all activities including query resolution, site closure and collection of documentation required for clinical trial reports after trail end;

4)      Ensuring all SAEs/AEs and protocol deviations are reported and followed up in a timely manner according to internal relevant SOP;

5)      Maintaining, updating and archiving all clinical trial files (site regulatory file and sponsor master file) on time;

6)      Managing study progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution;

7)      Any other responsibilities and duties which may be required from time to time.

You should have:

1)      A Bachelor's degree in a health care or other scientific discipline or educational equivalent

2)      Successful completion of a CRA Trainee Program or at least three months of on-site monitoring experience. At least 1-2 years of CRA experience, and capable of performing monitoring activities above independently.

3)      Alternatively, you should have an equivalent combination of education, training and experience. 

致力服务于医药行业。