Sign In
 [New User? Sign Up]
Mobile Version

RQMA, Technical Supervisor

Pfizer


Location:
Wuhan Shi, Hubei 430015
Date:
12/20/2017
2017-12-202018-01-20
Pfizer
Apply on the Company Site
  •  
  • Save Ad
  • Email Friend
  • Print
  • Research Salary

Job Details

**JOB SUMMARY**







+ Responsible for supporting Registry Data Quality and completeness by performing Quality Control on attributes submitted to the CTMS, utilizing data from within the system, as well as other systems (PTMF, ARGUS, EPM, iCTD) and source documents to validate the Registry Data Attributes, and will escalate any potential quality issue (missing or incorrect data).



+ Work with the Study Team Point of Contact to resolve any verified quality issues.



+ Work with RQM Lead, RQMA Leads, RQM PMBS Lead and CTMS OSMs to review and authorize any system business rule overrides required to correct the Registry Data Attributes.



+ Serve as the first point of contact for customers needing assistance with Clinical Trial Management System management questions and issues, and is to serve as a subject matter expert for the Registry process, related systems and tools.



+ Assist RQMA Leads in driving business solution for problem within the group, and/or in providing coaching/ direction to group member as designated.



+ Assist RQM PMBS Lead in managing business process(es) and performance, and/or driving project deliverables as designated.



+ Help maintain high standard of QC through enhancement initiatives in one or multiple subject matter(s).







**QUALIFICATIONS / SKILLS**







+ Qualifications Experience with web based data management systems.



+ Hands-on experience with Registry / Clinical Trial Management Systems



+ Experience with medical / clinical study records and documentation







+ Relevant experience in process management/task management is highly desirable.



+ Excellent performance in a customer service role with demonstration of meeting / exceeding customer needs.



+ Proven technical skills.



+ Experience and knowledge of ICH-GCP requirements



+ Experience in metrics management, preferably related to clinical trials Experience in database utilization.



+ Minimum of a Bachelor's degree or equivalent.



+ Good written and oral English skills.



+ Effective verbal and written communication skills in relating to colleagues and associates both inside and outside the organization.







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.
Apply on the Company Site
Powered ByLogo

Featured Jobs[ View All ]

Featured Employers [ View All ]