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Assocaite I, DM


Shanghai, R&d Center
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Job Details

+ Responsible for ensuring the completeness, quality and integrity of the subject data in the clinical trial database. And ensure data quality and consistency across programs and repositories.

+ Ensure the consistent use and application of applicable data standards following relevant SOP.

+ Responsible for data management activities within a clinical trial, according to regulations, applicable Standard Operating Procedures (SOPs) and Processes.

Works as one global study team to meet the study objectives.

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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