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Trial Data Programmer Bengaluru India,  


Posted on : 04 April 2017

Project Description

Requisition ID 45932BR Title Trial Data Programmer Job Category Biostatistics and Data Management Job Description Looking for Trial Data Programmer!!Are you a looking forward to take your career to the next level and give your career a new direction? Join Global Development GSC at Novo Nordisk to get a life-changing career and make a difference to thousand lives!!About the departmentGD-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 at Novo NordiskAt Novo Nordisk, 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.  State/Provinces Karnataka Position Location Bangalore Full Time or Part Time Full Time

Locations

India Bangalore

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