Data facilitation programmer

Department: Data Systems and Automation (DSA) Are you passionate about what you are doing? Do you want to build excellence within processes in the most efficient way? Do you have an innovative mindset to drive change in a future:ready environment? Are you best at what you do? If so, raise your hand as there is an exciting opportunity waiting for you as Data Facilitation Programmer with us. Apply Now At Novo Nordisk, we assure you will experience the best. About the department Data Systems and Automation (DSA), Data Management, Bengaluru is one of the most competent and diverse team of professionals who are mainly responsible for providing functional and system support to execute clinical trials across Product Development Plan portfolio. The team has strong understanding of Clinical Systems and interfaces with end:to:start mindset on standardisation of data:flow across systems, Electronic Case Report Form (ECRF) development using Central Designer and knowledge with Clinical Data Interchange Standards Consortium (CDISC) concepts annotated Case Report Form (aCRF), Study Data Tabulation Model (SDTM) mapping, SAS programming, Study Data Review Guideline (SDRG) etc., to aid CDISC submission which is a mandate from regulatory authorities. The Position As a Data Facilitation Programmer, you will be responsible for delivering/supporting solution for day:to:day operations or technical demanding tasks, wherein innovation is a key element. Data Facilitation Programmer will ensure consistency and knowledge sharing on the DM activities during clinical trial activities across projects. Ensure to target opportunities by systematically evaluating project needs, targeting those with the greatest potential for producing positive project results. Data Facilitation Programmer will be responsible for delivering/supporting solution for day:to:day operations or technical demanding task. : Responsible for execution of clinical trial data reports on Health tracker, EDC, Titration and Audit Trail reports as per trial squad requirements. : Facilitate data visualizations by creating custom listings in CDMS to aid better data review. : Perform mapping, testing, creating conversions and supporting DBL activities across interfaces. : Assist on programming and mapping activities to create Patient Status Dashboard for Clinical trials in a timely manner and to a high:quality level. : Data Facilitation Programmer will ensure consistency and knowledge sharing on the DM activities during clinical trial activities across projects. Hands:on programming experience in python or R with ability to solve visualization (Power BI). Experience : Masters / Bachelor s degree in Life Science or comparable degree in Computer science, Information Technology Clinical Information Management, or equivalent qualifications. : Minimum 2:4 years of experience in pharmaceutical industry and preferably 2 years within clinical data management systems. Relevant years of experience in pharmaceutical industry and preferably 2 plus years within clinical data management systems. : Understanding of protocol, CRF standards, Inform Terminologies and EDC data structure. : Knowledge and experience in Programming languages and experience in python or R with ability to solve visualization (Power BI). : Knowledge of computer systems, IT and clinical data process flow. : Knowledge of clinical development and basic medical terminology. : Experience in project management, collaboration, communication, and presentations skills. : Profound Knowledge of GxP and guidelines within drug development. Working At Novo Nordisk Novo Nordisk is a leading global healthcare company with a 100:year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacti