Senior Regulatory Professional developing regulatory strategies and leading execution via cross-functional teams for Novo Nordisk, focusing on Obesity and Diabetes portfolio.
Responsibilities
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.
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