Competency Development Specialist in Clinical Reporting

Location:

Søborg – Denmark

Salary:

Competitive

Type:

Permanent

Main Industry:

Search Health, Nursing & Social Services Jobs

Other Industries & Skills:

Manufacturing

Job ID:

132782380

Posted On:

19 March 2026

   

Competency Development Specialist in Clinical Reporting

Are you passionate about clinical process development and eager to drive process transformation? Do you have a profound understanding of clinical development and an end-to-end mindset?

Then you could be the one we are looking for. Join us as Competency Development Specialist and help to shape efficient, high-quality ways of working with clinical processes.

 

Your new role

As Competency Development Specialist, you’ll take ownership of a critical process, ensuring that SOPs, templates, and guidelines meet the regulatory requirements. This is a role where process excellence meets real impact, as the process you maintain are used daily by end-users across the globe to prepare documents that are essential for initiating clinical trials and securing drug approvals.

Your responsibilities will include:

style=”margin-top:0.0cm;margin-bottom:0.0cm” type=”disc”-
-Be content responsible for a process including authoring Standard Operating Procedures (SOP), guidance and templates (e.g., PI/IC forms or medical devices)
style=”margin-bottom:0.0cm;margin-top:0.0px”-
-Drive process changes that affect document preparation, incl. assessing emerging external requirements and their impact
style=”margin-top:0.0cm;margin-bottom:0.0cm” type=”disc”-
-Maintain efficient processes globally, and capture expert input to identify improvement opportunities
-Lead global competency development and training of end-users
-Act as process representative during external inspections and internal audits
style=”margin-bottom:0.0cm;margin-top:0.0px”-
-Build impactful stakeholder relationships to influence and leverage the evolving clinical process landscape
 

Your skills & qualifications

We’re looking for someone with strong pharmaceutical experience and a passion for process excellence who can lead through influence and collaboration.

You’ll bring:

style=”margin-bottom:0.0cm;margin-top:0.0px”-
-PhD or Master´s degree in science or equivalent
-Minimum 5 years of experience as a medical writer, regulatory specialist, QA professional, clinical operations or similar within the pharmaceutical industry
style=”margin-top:0.0cm;margin-bottom:0.0cm” type=”disc”-
-Experience working with clinical studies and regulatory requirements within drug and device clinical development
-Strong process orientation with excellent planning, coordination, and project management skills
-Experience with a broad range of different medical writing tasks, including structured authoring/content reuse
-Fluent in written and spoken English with strong communication and cultural awareness for working across global teams
 

In this role it is crucial to be able to manage complex stakeholder landscapes and drive consensus through negotiation and diplomacy while also work independently on larger projects, proactively identifying problems and suggesting solutions.

Your new department       

The position is based in the Clinical Reporting Process Excellence, Transparency, and Archiving Department in Søborg, Denmark, consisting of 13 dedicated colleagues. We share an interest in supporting our drug and device development projects with our specific areas of expertise. You will join the CR Process Excellence team that consist of 7 colleagues working on optimising processes, SOPs, and templates critical to clinical study documentation.

 

Working at Novo Nordisk

Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with determination, constant curiosity and a commitment to finding better ways forward. For over 100 years, this dedication has driven us to build a company focused on lasting change for long-term health. One where diverse thinking, shared purpose and mutual respect come together to create extraordinary results. When you join us, you’re not just starting a job – you’re becoming part of a story that spans generations.

 

More information

If you have additional questions about the position before applying, Rikke Juul Gøbel, Associate Director, on +45 34 44 60 01 or
RIGLnovonordisk

 

Deadline

6 April 2026. We look forward to receiving your application.

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.