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Trial Data Programmer - India  

Company managed [?] Still accepting applications

Posted on : 04 April 2017

Project Description


Description:
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About the department
  • GD-GSC-Data Management Unit supports Projects and Trial Management on operational Data Management activities of clinical projects. 
  • The key objective of the department is to ensure high quality data delivery to the stakeholders.
  •  The involvement of various groups in data management is significant in key stages of trial setup, conduct and closeout. 
  • The major activities handled include CRF Design, Database Programming, Data Entry, Data Validation, Medical Coding, Lab data handling, Data analysis & migration, Database Lock, Hyperlinking and Bookmarking and Project Management. 
  • These opportunities have in turn fostered a deeper understanding with an ability to drive, contribute to process and share best practices while leveraging cross-cultural collaboration towards a unified mission to achieve clean data GD-GSC-Data Management Unit supports Projects and Trial Management on operational Data Management activities of clinical projects. 
  • The key objective of the department is to ensure high quality data delivery to the stakeholders.
  • The involvement of various groups in data management is significant in key stages of trial setup, conduct and closeout. 
  • The major activities handled include CRF Design, Database Programming, Data Entry, Data Validation, Medical Coding, Lab data handling, Data analysis & migration, Database Lock, Hyperlinking and Bookmarking and Project Management. 
  • These opportunities have in turn fostered a deeper understanding with an ability to drive, contribute to process and share best practices while leveraging cross-cultural collaboration towards a unified mission to achieve clean data.



The position
  •  Develops programs and scripts including validation and derivation procedures used to support data management function to clean clinical data.
  • Create SAS views from OC raw data where applicable, Create views in OC, manipulate and transfer data files in the format required by customer. 
  • Ensure proper program testing and documentation, following appropriate SOPs, and data standards and to the right quality level. 
  • Adheres work to current DM standards: global validation/derivation procedures in OC/EDC.
  • Perform problem solving and troubleshooting for system procedures and processes that may arise in course of a clinical trial as related to the clinical database
  • Be able to export data or allow views of data from the clinical database to other systems in a secure and verifiable method.
  •  When necessary provide support for tools which require access to the clinical database.
  • Make data review listings and specialized reports on request as required.
  •  Responsible for the loading of external data into the clinical database.



Qualifications
  •  M.Sc / B.Sc in Computer Science / Life Science or comparable degree in Information Technology / clinical information management or equivalent qualifications.
  •  Minimum 2-3 years of experience in pharmaceutical industry and preferably 1 year within clinical data management systems
  •  Good Programming Skills on SQL and PL-SQL.
  •  Knowledge of clinical development and basic medical terminology
  •  Experience in project management, collaboration, communication and  presentations skills.



Working with Us:
  • We use our skills, dedication and ambition to help people with diabetes. 
  • We offer the chance to be part of a truly global work place, where passion and engagement are met with opportunities for professional and personal development.