Competency Development Specialist

Novo Nordisk; Gladsaxe Kommune; On-site; DKK 743,000 - 1,092,000; Full time

Benefits offered by this job

Incentives

Benefits

Job summary

Novo Nordisk in Søborg, Denmark, seeks a Content Responsible for the Medical Device Clinical Evaluation process to maintain SOPs, templates and training for stand-alone devices and drug-device combos, driving standardisation and digital adoption, including AI.

You will work across therapeutic areas to ensure compliant, efficient processes, and collaborate to enable integrated clinical workflows. Strong English and advanced degrees are required.

Qualifications

• PhD or Master’s degree in science or equivalent.
• Extensive and broad experience with medical device development and/or clinical development (MedTech or pharmaceutical).
• Experience with device clinical evaluation or related deliverables and regulatory requirements is an advantage.
• Strong drive, proactive stakeholder management, and a mindset for process innovation.
• Fluent in written and spoken English.

Responsibilities

• Act as content responsible for the Medical Device Clinical Evaluation process, authoring SOPs, guidance, templates and training.
• Collaborate to simplify and standardise the process for end users and leverage digital opportunities including AI.
• Ensure cross‑organisational knowledge sharing and efficient processes across therapeutic areas.
• Support quality processes across Clinical Reporting units during inspections and audits, SOP reviews and impact assessments.
• Assist the Clinical Reporting Process Excellence department and contribute to training and competency development.

Skills

English fluency

Stakeholder mgmt

Process mindset

Digital innovation

Education

PhD or Master’s in science

Job description

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

If so, then you might be our new colleague in the Clinical Reporting Process Excellence department. The position offers a unique opportunity to improve the medical device clinical process to leverage best practices and digital innovation to the benefit of our global organisation.

In this role, you will act as Content Responsible for the Medical Device Clinical Evaluation process, maintaining and improving its Standard Operating Procedures (SOPs), guidance, templates and training for stand‑alone medical devices and drug‑device combination products. The focus will be on maintaining a well‑functioning and compliant process for end‑users as well as driving simplifying and standardisation of the process, enabling the implementing digital technologies. You will be part of the Clinical Reporting Process Excellence department and collaborate to provide important input to clinical processes across drug and device to facilitate and build integrated processes and a fit‑for‑purpose approach.

Your Main Tasks Will Include

• Acting as content responsible for the Medical Device Clinical Evaluation process including authoring SOPs, guidance, templates and training.
• In close collaboration with the Process Manager, identifying and implementing improvements to simplify and standardise the process for the end‑users and leverage digital opportunities incl. AI use.
• Securing department, cross‑organisational knowledge‑sharing, and collaborating to ensure operational and efficient processes across therapeutic areas.
• Supporting quality processes across Clinical Reporting units in connection with external and internal inspections and audits, SOP review and impact assessment.
• Assisting across the Clinical Reporting Process Excellence department and functioning as Clinical Reporting representative in working groups and networks. Driving competency development in Clinical Reporting.

Skills And Qualifications

• PhD or Master´s degree in science or equivalent
• Extensive and broad experience with medical device development and/or clinical development in the MedTech or pharmaceutical industry; e.g. medical writing, regulatory affairs, process ownership or other relevant work.
• Broad range of experience within different medical writing tasks, including structured authoring/content reuse. Experience in working with device clinical evaluation or related deliverables and applicable regulatory requirements is considered an advantage.
• Strong drive and proactive stakeholder management skills, and a mindset that fosters process innovation and fit for purpose solutions
• Fluent in written and spoken English.

As a person, you are a natural team player, thrive in a complex work environment and bring a can‑do‑spirit and a passion to drive change. You are a flexible and change‑oriented person with strong analytical skills, who can work independently on larger tasks. Further, it is important for you to be an active contributor to the success of the entire team.

About The Department

The position is based in Søborg, Denmark, where we are a team of dedicated colleagues committed to ensuring competency among our global colleagues who work on our drug and device development projects. Additionally, we have a shared interest in innovation and digitalisation incl. use of AI in Clinical Reporting Processes.

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.

What We Offer

At Novo Nordisk, you’ll join a global healthcare company with a unique culture and strong results. We offer continuous learning, career development, and benefits tailored to your life and career stage.

Salary:

For this role, the Annual Base Salary ranges from 742,600.00 to 1,091,600.00 DKK, corresponding to the level of the position.

Incentives and Benefits:

The salary package may include short‑term and/or long‑term incentives as well as other employee benefits based on position level, location, functional area and relevant market benchmarks.

Learn more about our Reward Philosophy here.

Deadline

16th September 26

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.