Clinical Supplies Set-Up Professional (Denmark, Måløv)

Jobbeskrivelse
Placering
Måløv, Denmark

Jobkategori
Clinical Development

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Are you passionate about clinical trials? Do you want to ensure the smooth execution of clinical supplies? We are looking for a dedicated Clinical Supplies Set-up Professional to join our team at Novo Nordisk. If that sounds like you, read on and apply today for a life-changing career.

The position
As Clinical Supplies Set-up Professional you will join a team of dedicated professionals.

Your main responsibilities will include:

• Ensuring clinical supply input to clinical trial protocols

• Creating trial master data, clinical label text and trial specific manuals to be used by clinical sites and aligned with products specifications and regulatory requirements

• Ensure documents are ready for clinical trial application to authorities

To succeed in the job, you will establish and maintain collaboration with a wide range of stakeholders across Novo Nordisk. Furthermore, you will together with experienced colleagues be empowered to develop and improve processes.

Qualifications
To succeed in this role, you have:

• MSc degree in Natural, Health or Pharmaceutical Sciences or similar

• Experience in the pharma industry will be a plus

• Quality mindset and experience with regulatory requirements, e.g., GCP and GMP.

• Data-driven, analytical, and methodical capabilities with flair for IT systems and tools.

• Excellent collaboration and communication skills with fluency in English.

As a person you take pride in consistently delivering high-quality work on time and in a pro-active way. On top of that, you can prioritise your assignments in an ever-changing and dynamic environment. You are a team player, who aspire to continuously learn and take challenges as opportunities to grow.

About the department
The Clinical Supplies Trial Set-up department consists of six teams who prepare clinical trials for supply execution by forecasting product demand, simulating trial supply execution, setting up supply systems and preparing regulatory documents for CTA.

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
For further information, please contact Senior Manager Kristine Beisner at +45-30753767.

Deadline
Apply before 27 October 2024

You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV.

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.