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.
