Biostatistical Specialist for Clinical Development in Copenhagen or Aalborg

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Søborg

  • Clinical Development and Medical
  • Søborg

Do you wish to work in a highly professional, engaging and global environment where you can use your statistical expertise and quality mindset to bring clinical projects to registration and market? Then you may be our new Statistical Specialist to join our Søborg or Aalborg site.

About the department

The Biostatistics function currently consists of approximately 250 statisticians and statistical programmers globally. Of these, 170 are situated in Denmark, where we are organised in departments supporting our development projects (e.g. GLP-1, Insulin, Haemophilia or Obesity). The Biostatistics function consists of statisticians and statistical programmers in roughly equal split.

Novo Nordisk has a broad R&D pipeline and majority of our statistical work is done in-house, thus we offer a wide variety of statistical challenges and provide a strong scientific community. We are organised in smaller units for each clinical project to ensure close collaboration with our various stakeholders.

The position

In the “Biostatistics Insulin & Devices” department, we are looking for a statistical specialist to take a key role in the planning and execution of a new phase 3 programme. One of the immediate tasks is to give input to the analytical specifications on project level as well as to the individual phase 3 trials (i.e. input to protocols, analysis plans and project analysis plan) and drive alignment of protocols with relevant consideration for adjacent projects. You will work closely together with medical staff, health economists, the International Project Statistician and the International Lead Programmer. The task also include collaboration to ensure proper collection and reporting of data collected via digital tools like connected real time devices.

As a statistical expert you will be providing statistical advice to development plans, input to trial designs and protocols, support the creation of trial reports, summary documents, support answering questions from regulatory authorities and prepare publications, etc. You will be involved in presentations and discussions of results both internally and externally and participate in meetings with regulatory authorities and external collaborators.

Coaching of less experienced colleagues is a natural part of the job and we expect you to be able to communicate statistical problems and ideas clearly to both statistical colleagues as well as stakeholders from other functional areas.

Development of methods and processes as well as knowledge sharing is continuously on-going in Novo Nordisk, especially based on the initiative of the employees. We expect you to take part in our dedicated efforts to make Biostatistics, globally, a good and challenging place to work. In exchange we offer great opportunities for on-going training to ensure your continued competency development.

Qualifications

You have a solid theoretical background in statistics corresponding to at least MSc level and at least five years of experience within clinical or bio-statistical research. You have excellent programming skills and attention to details. You must be able to act as driver and leading member of the project teams you are part of, and if you have experience from project management and supervision of colleagues, it will be an advantage. You must thrive in a role where you independently and proactively set direction for your part of the projects while handling several challenging tasks in parallel without compromising the quality of your work. As such, you must be able to create overview, prioritise and bring a flexible and positive mindset when things are moving fast, and deadlines are closing in. It will be advantage if you have experience with phase 1 trials.

Global Development is an organisation with many international employees, and we welcome non-local applicants.

Research & Development is vital to Novo Nordisk’s continuous growth. Your ambition and passion are therefore essential to achieve our goal of creating better lives for people living with chronic diseases. That is why working here is rewarding for us – and for you.

Contact

For further information, please contact Peter Falck Christens (+45 3079 9440) or Morten Kanneworff (+45 3079 0573).

Deadline

March 1st, 2020. Please notice that applications will be processed as they are received. Please note in your application whether you are interested in working at our site in Søborg or Aalborg.

Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.


Information og data

Denne ledige stilling har jobtypen "Laborant", og befinder sig i kategorien "Sundhed og forskning".

Arbejdsstedet er beliggende i Søborg.

Jobbet er oprettet på vores service den 3.2.2020, men kan have været deaktiveret og genaktiveret igen.

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Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
  • Laborant
  • Søborg
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