.Do you have solid experience in clinical development or biostatistics?
Are you eager to work in a highly professional, engaging, and global environment where you can use your programming skills and scientific expertise and help bring clinical projects to market?
Do you want to join us in the journey of becoming more innovative and to change lives for a greater number of people living with serious chronic diseases?
If so,then consider this great opportunity and join us for a life: Based in Madrid or home: Based in different locations in Spain.The position As a Statistical Programmer Specialist, you can be expected to solve tasks ranging from being a trial programmer on one or more simultaneous trials to being the main programming responsible for submission of trials and input to summaries, including leading the Authority Q and A and inspection sessions within a program.
You will then need to be a programming specialist with profound and broad clinical development knowledge and experience.
Experience working with CDISC standards for submission as well as understanding coding of trials of high complexity is a necessity.
You may also become a driver of a working group e.G., with a focus on data visualisations, if you have experience within this area as well as extraction of data insights aiming at efficient trial closure and optimizing submission related activities.
All activities will be performed in close collaboration with both your biostatistics colleagues and stakeholders such as Data Management, Medical Writers, and Medical Doctors: Collaboration and stakeholder management skills are therefore important.Qualifications Being a Statistical Programming Specialist at Novo Nordisk requires profound domain expertise and the wish to constructively challenge existing standards, a result-oriented working style with sufficient expertise to break down issues into practical solutions, and sufficient business understanding of stakeholder dependencies and requirements to optimise the business results.
As a specialist, you can easily explain difficult technical issues to peers and actively seek and act on feedback from others.As a minimum, you meet the following requirements:MSc, PhD in Natural or Technical Sciences (or equivalent theoretical background)5 years of experience within clinical development or biostatisticsAct as driver and leading member of the project teams you are part ofIndependently and proactively set directionExpert programmer within SAS, R and/or PythonAbout the department Biostatistics is a part of the Data Science organization and counts 250 statisticians and statistical programmers globally.
In Biostatistics, we are organised in smaller units within clinical therapeutic areas ensuring close collaboration with our various stakeholders.
Primarily we perform our statistical programming work in-house, thus we offer a wide variety of tasks and challenges and provide a strong scientific community