Senior Regulatory Professional – Temporary Position (2 years)
Novo Nordisk
full-time
Posted on:
Location Type: Office
Location: Søborg • 🇩🇰 Denmark
Visit company websiteJob Level
Senior
About the role
- responsible for driving several regulatory tasks with challenging and often overlapping timelines
- member of cross functional project and submission teams
- interact with a variety of stakeholders
- responsible for the development of regulatory documentation
- contribute to the global regulatory strategies and tactics
- engage in authority interactions and planning for regulatory approval
Requirements
- master’s degree in life science
- 4-5 years of regulatory or drug development experience
- background within Research or Clinical Drug Development
- skilled communicator
- fluent written and spoken English
Benefits
- flexible set-up
- trust & openness
- sparring
- challenge
- knowledge sharing
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
regulatory documentationregulatory strategiesregulatory approvaldrug development
Soft skills
skilled communicatorinterpersonal skills
Certifications
master’s degree