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Senior Clinical Data Coordinator

$20/hr Starting at $100

Data Management MS Excel MS Word MS Power Point PDF Tamil CDM Experience: • Recognize, exemplify and adhere to company’s values which center on our commitment to People, Clients and Performance. • As a member of staff, the employee is expected to recognize the importance of and create culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs. • Read, ensure understanding and adhere to all assigned Company’s SOPs and working procedures. • Ensure all work performed is of high quality, compliant with Good Clinical Practice, ICH Guidelines and all applicable laws and regulations. • Complete all assigned trainings (including the Study Lead Development program) and courses in the Company’s Training Management system (iLearn); ensuring that mandatory courses are all completed before the designated date and that the required system specific training has been completed for current studies. • Record all billable and non-billable time in the appropriate timesheet management system (e.g. Planview™). • Review CRF I eCRF data for completeness, accuracy, and consistency via computerize edits and manual data checks. • Perform external data reconciliation. • Perform Serious Adverse Event reconciliation. • Generate and close/resolve (as appropriate) data queries. • Freeze and/or lock eCRFs (as appropriate) within the Electronic Data Capture System. • Create and maintain study files and other appropriate study documentation. • Perform User Acceptance Testing and collaboratively work with CDMS personnel to see issues found through re-testing and resolution. • Assist Data Management Study Lead in development of eCRF, Data Validation Specifications, and Study Specific Procedures. • Train and guide less experienced CDCs in data management requirements and activities. • Perform other project activities as required in order to ensure that study timelines are met (for example, filing and archiving of study documentation, dispatching of queries to investigator or sites for resolution, etc.). • As required, communicate effectively with the Project team, Study Lead, Project Lead and Project Manager. • Leading Microsoft Excel forum • Point of Contact for Locking and Freezing task through BOT • Point of Contact for Country level Clinical Data Coordinators Metrics. Written many poems, short stories in Tamil.

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$20/hr Ongoing

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Data Management MS Excel MS Word MS Power Point PDF Tamil CDM Experience: • Recognize, exemplify and adhere to company’s values which center on our commitment to People, Clients and Performance. • As a member of staff, the employee is expected to recognize the importance of and create culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs. • Read, ensure understanding and adhere to all assigned Company’s SOPs and working procedures. • Ensure all work performed is of high quality, compliant with Good Clinical Practice, ICH Guidelines and all applicable laws and regulations. • Complete all assigned trainings (including the Study Lead Development program) and courses in the Company’s Training Management system (iLearn); ensuring that mandatory courses are all completed before the designated date and that the required system specific training has been completed for current studies. • Record all billable and non-billable time in the appropriate timesheet management system (e.g. Planview™). • Review CRF I eCRF data for completeness, accuracy, and consistency via computerize edits and manual data checks. • Perform external data reconciliation. • Perform Serious Adverse Event reconciliation. • Generate and close/resolve (as appropriate) data queries. • Freeze and/or lock eCRFs (as appropriate) within the Electronic Data Capture System. • Create and maintain study files and other appropriate study documentation. • Perform User Acceptance Testing and collaboratively work with CDMS personnel to see issues found through re-testing and resolution. • Assist Data Management Study Lead in development of eCRF, Data Validation Specifications, and Study Specific Procedures. • Train and guide less experienced CDCs in data management requirements and activities. • Perform other project activities as required in order to ensure that study timelines are met (for example, filing and archiving of study documentation, dispatching of queries to investigator or sites for resolution, etc.). • As required, communicate effectively with the Project team, Study Lead, Project Lead and Project Manager. • Leading Microsoft Excel forum • Point of Contact for Locking and Freezing task through BOT • Point of Contact for Country level Clinical Data Coordinators Metrics. Written many poems, short stories in Tamil.

Skills & Expertise

Data ManagementMicrosoft ExcelMicrosoft PowerPointMicrosoft WordPDF Design

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