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Asso. I, RQM

Pfizer


Location:
Wuhan Shi, Hubei 430015
Date:
11/27/2017
2017-11-272017-12-28
Pfizer
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  • Research Salary

Job Details

**JOB RESPONSIBILITIES**







+ 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.







**QUALIFICATIONS / SKILLS**







+ 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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