Medical Device Clinical Process Innovator

Novo Nordisk A/S; Søborg; On-site; DKK 743,000 - 1,092,000; Full time

Job summary

Novo Nordisk A/S in Søborg, Denmark, is seeking a Content Responsible for the Medical Device Clinical Evaluation process within the Clinical Reporting Process Excellence department. The role focuses on maintaining SOPs, guidance, templates, and training for stand-alone devices and drug-device combinations, while driving standardisation and digital innovations.

The position collaborates across drug and device processes to enable integrated, fit-for-purpose clinical workflows and to support

Qualifications

• PhD or Master’s degree in science or equivalent required.
• Extensive experience with medical device development or clinical development.
• Experience in medical writing, regulatory affairs, or process ownership is a plus.
• Fluent in written and spoken English.

Responsibilities

• Content Responsible for the Medical Device Clinical Evaluation SOPs, guidance, templates and training.
• Collaborate to simplify and standardise the process and leverage digital opportunities incl. AI use.
• Support quality processes across Clinical Reporting units and assist in inspections and audits.
• Represent Clinical Reporting in working groups to drive competency development.

Skills

Medical device development

Clinical development

Medical writing

Regulatory affairs

Stakeholder management

English proficiency

Education

PhD or Master’s degree in science

Job description

Novo Nordisk A/S in Søborg, Denmark, is seeking a Content Responsible for the Medical Device Clinical Evaluation process within the Clinical Reporting Process Excellence department. The role focuses on maintaining SOPs, guidance, templates, and training for stand-alone devices and drug-device combinations, while driving standardisation and digital innovations.

The position collaborates across drug and device processes to enable integrated, fit-for-purpose clinical workflows and to support