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.
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 - 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.