Pfizer Asso. II, RQM in Wuhan, China


  • Upon direction, run and review the Registry Quality Management reports or other logic check mechanisms throughout clinical study life.

  • Investigate logic check flags, utilizing system information, as well as applicable study documentation.

  • Review data attributes populated by general users for adherence to Registry Data Quality Specifications.

  • Identify and investigate any potential discrepancies Review findings with the study team Point of Contact to verify data quality issues.

  • Create, modify or delete data attributes in the CTMS system according to Registry Data Entry specifications.

  • Generate required metrics for each study.

  • Function as subject matter expert for Registry systems and tools.


  • Excellent English verbal and written communications skills and outstanding listening skills are required.

  • History of achievement in a customer service role with demonstration of meeting customer needs and concerns required.

  • Proven history of leadership roles within a team environment required.

  • Experience with Clinical Trial Management Systems preferred.

  • Experience in management of medical/clinical study records and documentation preferred.

  • Experience/knowledge of ICH/GCP documentation requirements preferred.

  • Metrics management experience (preferably within the field of Clinical Research) preferred.

  • Experience with web based data management systems preferred.

  • Experience with database utilization preferred.

  • Minimum of Bachelor's degree or equivalent required.

N: Not Applicable - 不适用 (China)

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.