Data Facilitation Programmer
4 weeks ago
Data Facilitation Programmer
Department: Data Systems & 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 & 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 & 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 & 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
At Novo Nordisk, we are driving change to defeat diabetes and other serious chronic conditions. Our treatments today are benefiting millions of people living with diabetes, obesity, and rare blood and endocrine diseases. From our labs to our factory floors, we are discovering and developing innovative biological medicines and making them accessible to patients throughout the world. Since the company was founded in Denmark more than 100 years ago, we have been translating the unmet medical needs of people living with serious chronic diseases into innovative medicines and delivery. Our focus is on these diseases, which affect hundreds of millions of people and are among the most urgent global health challenges. By combining our innovation and commercial excellence, we draw upon insights from patients and partners to transform bold ideas into life-saving and preventive medicines. Our ambition is to take the lead in each of these areas, driving change with an unfailing belief that it can be done.
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