- Location:
- Søborg – Denmark
- Salary:
- Competitive
- Type:
- Permanent
- Main Industry:
- Search Information Technology Jobs
- Other Industries & Skills:
- Advertising, Marketing & PR, Health, Nursing & Social Services Legal, Science
- Job ID:
- 132662779
- Posted On:
- 29 January 2026
Are you skilled at driving process transformation that makes complex work simpler and faster? Are you passionate about building strong stakeholder relationships? And do you excel at setting direction to align process innovation with Clinical Reporting content strategy?
Then you could be the one we are looking for. Join us as a Process Simplification Principal Specialist and help shape efficient, high-quality ways of working.
Your new role
As Process simplification principal specialist you will be responsible for:
style=”margin-bottom:0.0in;margin-top:0.0px”-
-Drive simplification, standardisation and optimisation of SOPs, templates and guidance documents anchored in Clinical Reporting
-Set direction to align process innovation with Clinical Reporting content strategy
-Amplify impact by nurture a process transformation mindset in colleagues, stakeholders and across Clinical Reporting
-Build impactful stakeholder relationships to influence and leverage the evolving clinical process landscape
Your new department
The position is within the Clinical Reporting Process Excellence, Transparency, and Archiving Department in Søborg, Denmark, consisting of 14 dedicated colleagues. We share an interest in supporting our drug development projects with our specific areas of expertise. You will join the Process Excellence team that consist of 7 colleagues working on optimising the Clinical Reporting owned processes within the evolving clinical process landscape.
Your skills & qualifications
We’re seeking candidates who fulfil the following prerequisites:
style=”margin-bottom:0.0in;margin-top:0.0px”-
-You hold a PhD or master’s degree in science (or equivalent)
-You have minimum 5yrs experience operating and preferably driving change in a complex process and quality landscape
-You have minimum 6yrs experience as a medical writer or other relevant role in the pharmaceutical industry
-You have minimum 3 years’ experience with teaching, training or mentoring
-You have a deep understanding of regulatory processes, documentation requirements and the clinical development value chain
-You demonstrate the ability to identify better practice, challenge the status quo and drive improvement
-You demonstrate the ability to collaborate and influence in international and diverse professional groups
-You are fluent in written and spoken English
As a person you are highly independent and take ownership of complex tasks, proactively resolving issues and staying flexible in uncertainty. You plan and prioritise multiple competing activities for yourself and others, apply strong analytical thinking, and remain committed, persistent and accountable. You communicate clearly and respectfully, foster collaboration across multidisciplinary and global teams, and influence others through mentorship and informal guidance. You drive strategic discussions aligned with Clinical Reporting, build relationships with decision-makers, and lead initiatives to deliver on Clinical Reporting objectives.
Working at Novo Nordisk
Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with an unconventional spirit, a rare determination and a constant curiosity. For over 100 years, this unordinary mindset has seen us build a company unlike any other. One where a collective passion for our purpose, mutual respect and a willingness to go beyond what we know delivers extraordinary results.
What we offer
There is, of course, more on offer here than the uniqueness of our culture and the extraordinary results we produce. Being part of a global healthcare company means opportunities to learn and develop are all around us, while our benefits are designed with your career and life stage in mind.
More information
If you have additional questions about the position before applying, Rikke Juul Gøbel, Associate Director, on
RIGLnovonordisk
Deadline
15th of February 2026.
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 will be reviewing application on an ongoing basis, so please submit your application at your earliest convenience.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk, we’re not chasing quick fixes – we’re creating lasting change for long-term health. For over 100 years, we’ve been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what’s possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we’re making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.
To help us track our recruitment effort, please indicate in your email/cover letter where (vacanciesineu.com) you saw this job posting.
