Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. In addition to your competitive salary, ICON offers a range of additional benefits. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. Our success depends on the quality of our people. Deliver Higher-Quality Data, Faster and with Less Effort, Cost and Risk. Responsible for archiving trial(s) and associated documentation upon trial(s) completion.Įnsure adherence to Good Clinical Practice and all applicable local and international regulations. Oracle Health Sciences InForm EDC Platform. Perform data review and discrepancy resolution, as needed. Oncology and/or inflammatory therapeutic area experience is preferred. Clinical Data Coordinators that are supporting their trial(s). Experience with Oracle Inc.s Inform EDC system is preferred. Responsible for providing data review training and guidance to Sr. Responsible for working with the assigned Clinical Database Programmer(s) to ensure the development of the Data Flow Chart(s), Data Transfer Specifications and Import Guidelines.Īssist with site and/or third party vendor training on CDM-related topics. Participate in Quality Control (QC), as needed. Participate in User Acceptance Testing (UAT), as needed. Responsible for the review, development and/or writing of clinical trial documents and manuals, including but not limited to Case Report Forms, Edit Checks, Data Management Plans, Clinical Data Review Plans and eCRF Completion Guidelines. Responsible for communicating key clinical data management metrics (e.g., data entry status, query resolution and aging, etc.) and determining appropriate actions in conjunction with study team. Everest builds InForm databases in-house, including designing eCRFs, programming of simple and complex data validation check, and data integration with IWRS/IVRS and other clinical trial management and safety. Participate as the primary data management representative on multidisciplinary project teams and ensure effective communication exchange. InForm is one of the industry brand name EDC systems, offering an intuitive user interface, and comprehensive role-based online training. The CDM ensures, from a data management perspective, assigned trials on time, within budget, and with highest achievable quality. All rights reserved.The Clinical Data Manager performs activities pertaining to the conduct of Phase I – III clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant procedures and guidelines. Copyright © 2013 Oracle and/or its affiliates. For example, in the Cognos documentation, report topics are referred to as query subjects and report elements are referred to as query topics. Note: References to Query Studio and queries have been removed from the Reporting and Analysis user interface and documentation to avoid confusion by clinical users to whom the term query means a clinical discrepancy, not a database operation. ![]() Ad hoc reports allow limited use of Cognos features such as data output styles, report layout and formatting, summarizations and aggregations, mathematical functions, and prompts. You create ad hoc reports on both clinical and study management data using the InForm Ad Hoc Reporting workspace. ![]() Remember that you can use Oracle Clinical One Analytics whether you are working in a brand new or existing study. ![]()
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