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Asso. II, RQM


Wuhan Shi, Hubei 430015
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  • Research Salary

Job Details


+ 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 - (China)

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