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| Job Location | Hyderabad |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Medical / Healthcare |
| Functional Area | General / Operations Management |
| EmploymentType | Full-time |
This position is responsible for undertaking and reviewing the technical activates required to build, test, maintain and archive clinical study databases throughout the duration of a study, this position may also act as the lead CDMP on simple studies.Major Responsibilities: Create annotated e case report forms(eCRF)Build test and maintain databases.Create and test data entry screens.Program and test files necessary for the electronic upload of data.Upload electronic data received through external sources.Program and generate data listings for ongoing studies.Program and generate project tracking reports.Perform data transfers.Archive electronic data and required doc on study completion.Act as programming contact with sponsor to address database issues regarding or relating to area of expertise.Communicate the database set-up status and the achievement of milestones to internal or external project team members.Track milestones and issue status reports.Responsible for performing activities that are in compliance with applicable corporate and divisional policies, standard operating procedures and operating guidelines and performing other duties as assigned by management.Minimum Experience:
Keyskills :
compliancemajorprogrammingmanagementenvironmentcommunicationdesignreportskillsinterpersonaldataentryprojectdatabaseclinicaltracking