Data Facilitation Programmer

Data Facilitation Programmer

**Category**:Data & AI**Location**:Bangalore, Karnataka, IN**Department**:Data Analytics & Facilitation, Clinical & Data Science, Bangalore Global Development GBS-
**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. Should perform independently and in accordance with Novo Nordisk SOPs, Novo Nordisk policies and the Novo Nordisk Way.- 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.

**Experience**
- Masters / Bachelor’s degree in Life Science or comparable degree in Computer science, Information Technology Clinical Information Management or equivalent qualifications.
- 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.
- 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 don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales
- we're all working to move the needle on patient care.**Contact**-
**Deadline**- We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.- At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.