Novo Nordisk

Senior Regulatory Professional

Novo Nordisk

full-time

Posted on:

Location Type: Office

Location: Søborg • Denmark

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Job Level

Senior

About the role

  • Take part in developing regulatory strategies and lead execution via interactions with cross-functional teams
  • Participate in the development of regulatory documentation for submission to Health Authorities
  • Provide regulatory input, being proactive and challenging the assumptions while contributing to project team decisions
  • Interact with medical and non-clinical specialists, statisticians, and medical writers
  • Report to the head of the department and take active part in department related activities

Requirements

  • A Master’s degree or Ph.D. in science, pharmaceutical or health science
  • Minimum 5 years of experience in the pharmaceutical industry
  • Solid and hands-on regulatory experience
  • Excellent project management skills and ability to cooperate at any organizational level
  • Change-oriented approach and a willingness to experiment
  • Strong communication skills in verbal and written English.
Benefits
  • Flexible working hours
  • Professional development opportunities
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
regulatory strategiesregulatory documentationproject managementregulatory experience
Soft Skills
communication skillscooperationchange-oriented approachproactivedecision making
Certifications
Master’s degreePh.D.