Job Description
•Independently responsible for all data processing tasks and deliverables on assigned data processing projects including:
-Development of database build specifications
-Development of data validation specifications
-Test data creation & UAT
-Performing/ leading functional QC activities and testing
-Create CRF Completion Guidelines (CCG), SAE reconciliation Guidelines, etc.
-Data validation and cleaning
-Conduct medical coding if assigned
-Conduct SAE & third party data reconciliations
-Perform early and final database QC activities
-Database lock activities
-Maintaining Clinical Study Documents and archiving as appropriate
•Responsible for completeness, timely delivery and quality of clinical data
•Lead and coordinate other team members within the department on moderately assigned studies or multiple small protocols
•Mentor project team members and be a subject matter expert when needed
•Represent Data Management (DM) function in external client meetings and presentations such as investigator meetings as required. May represent PAREXEL at professional meetings / conferences
•Other assigned responsibilities as needed
•Independently responsible for all data processing tasks and deliverables on assigned data processing projects including:
-Development of database build specifications
-Development of data validation specifications
-Test data creation & UAT
-Performing/ leading functional QC activities and testing
-Create CRF Completion Guidelines (CCG), SAE reconciliation Guidelines, etc.
-Data validation and cleaning
-Conduct medical coding if assigned
-Conduct SAE & third party data reconciliations
-Perform early and final database QC activities
-Database lock activities
-Maintaining Clinical Study Documents and archiving as appropriate
•Responsible for completeness, timely delivery and quality of clinical data
•Lead and coordinate other team members within the department on moderately assigned studies or multiple small protocols
•Mentor project team members and be a subject matter expert when needed
•Represent Data Management (DM) function in external client meetings and presentations such as investigator meetings as required. May represent PAREXEL at professional meetings / conferences
•Other assigned responsibilities as needed
Candidate Profile
Must be able to demonstrate proficiency with all tasks from data start-up through data-base lock. Previous relevant data management work experience of 3-6 years required; clinical and/ or research experience with solid understanding of clinical trials methodology and terminology required.
Additional Information:Must be able to demonstrate proficiency with all tasks from data start-up through data-base lock. Previous relevant data management work experience of 3-6 years required; clinical and/ or research experience with solid understanding of clinical trials methodology and terminology required.
Experience: 3-6 years
Location: Andhra Pradesh - Hyderabad
Functional Area: CR
Requisition: pare-10033584
Industry Type: Pharma/ Biotech/Clinical Research
Employment Type: Full Time
Job Type: Regular
End Date: 30th June, 2014
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