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lastModificationDate: 1544446271710

stillingsbetegnelse:
Programming Specialist responsible for high impact applications

jobbeskrivelse:

Do you want to be part of a dynamic team responsible for programming high impact applications across projects in Novo Nordisk? Do you thrive by working in an international environment and are you prepared to embrace and tackle challenges as part of your work each day? Are you structured, have good planning skills and have a mind-set for optimisations? Then we may have the right job for you.

In Global Development, we are responsible for managing clinical drug development worldwide from early development phases to product introduction. We provide medical and scientific documentation for clinical submissions and authorities and ensure that the process lives up to uniform global standards, regulations and business ethics. We work in Global Project teams with focus on delivering viable products that make a difference to patients and ultimately benefit society.

About the department
Clinical Data Standards (CDS) is a part of Global Development and our main responsibility is to develop standards for collection and reporting of clinical data ensuring that Novo Nordisk submits data and documents in compliance with regulatory requirements. We support the use of clinical data standards from early trial design to submission of data and documentation in accordance to the international data standard Clinical Data Interchange Standards Consortium (CDISC).

Our department consists of 27 enthusiastic and highly engaged people working closely with multi-functional and international teams on a variety of clinical and technical projects in a pleasant and informal atmosphere.

The position
As Programming Specialist in CDS you will be part of a team of programming experts responsible for development and optimisation of a variety of tasks. These tasks span from stand-alone programs to bigger applications, all supporting the production of CDISC compliant data and reporting to support business deliverables and review/approval processes for all clinical trials in Novo Nordisk. This entails driving the programming efforts and system implementation needed when upgrading to new data and terminology versions or when optimising the program library to align with industry best practices.

Besides programming you will be part of driving the development and maintenance of clinical data standards and related processes in alignment with the needs from clinical projects, clinical systems and processes, external regulatory requirements and industry best practices and you will take part in multi-stakeholder data standardisation projects.

You will have close collaboration with our primary stakeholders such as Biostatistics, Data Management, Study Data Tabulation Model (SDTM) Programmers, Risk Based Monitoring and Trial Management in order to define optimal data standards to be used across clinical projects in Novo Nordisk.

Qualifications
You have a B.Sc., M.Sc. or Ph.D. within IT, Natural Sciences or other relevant degree and you bring 5-8 years of extensive knowledge of and experience with advanced programming. Preferably you have experience with SAS programming, driving IT projects and IT system development methodologies.

We expect you to be structured and efficient combined with an ability to manage several challenging tasks in parallel without compromising quality. Furthermore we work in an environment where we occasionally need to drop everything and gather high performance teams to solve burning issues in the organisation, so a degree of agility and flexibility is also needed.

The job requires that you are able to work in a team with diverse skill sets and varying levels of expertise with clinical data standards. You will play an important role in the ongoing competency development of and support to the department and its many stakeholders.

As a specialist we expect you to be a driver, show initiative, work independently, seek guidance when needed and take responsibility for delivering high-quality results on time. Since you will be working in an international setting we expect you to be fluent in English, written and spoken.

 

Working at Novo Nordisk

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information, please contact Martin Lindhard at +45 3075 1060 or Trine Næstoft at +45 3075 2135.

Deadline

January 6, 2019

 

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.

numberOfPosts: 1

jobCategoriesCodes_0: http://data.europa.eu/esco/isco/C2512

abstractJV_contact_0: Please apply using one of the specified channels

positionTypeCode: directhire

contractTypeCodes_0: fulltime

Arbejdsgiver Navn: Novo Nordisk A/S

source: DK-STAR