Emma Cheesman-Ungstrup Email
Director of Development Consulting and Scientific Affairs @ Biopharma Excellence
Emma Cheesman-Ungstrup's Location
Copenhagen, Capital Region, Denmark
Emma Cheesman-Ungstrup's Work
- Director of Development Consulting and Scientific Affairs @ Biopharma Excellence
- Associate Director Regulatory Affairs @ ERA Consulting
- Director of Regulatory Affairs @ IO Biotech
- Senior Regulatory Professional, Regulatory and Medical @ LEO Pharma
- Regulatory Strategy Leader @ Lundbeck
- Toxicologist @ Sanofi Pasteur
- Product Manager Regulatory Development @ Sanofi Pasteur
- Lab Head in in Vivo Toxicology @ Addex Therapeutics
- Regulatory Affairs Manager @ ERYTECH Pharma
- Head of Non Clinical Development @ Jazz Pharmaceuticals
Emma Cheesman-Ungstrup's Education
- Københavns Universitet - University Of Copenhagen
(Economics)
2017 - 2017 - University of Otago
Bachelors (French Language, Literature, French Language and Literature)
2008 - 2009 - University of Otago
Bachelor of Science (Biochemistry)
1993 - 1997
Emma Cheesman-Ungstrup's Skills
- Pharmaceutical Industry
- Clinical Development
- Drug Development
- Regulatory Submissions
- Biotechnology
- Clinical Trials
- Drug Discovery
- Toxicology
- CRO
- In Vivo
Emma Cheesman-Ungstrup's Summary
Emma Cheesman-Ungstrup, based in Copenhagen, Capital Region, Denmark, is currently a Director of Development Consulting and Scientific Affairs at Biopharma Excellence, bringing experience from previous roles at Era Consulting, Io Biotech, Leo Pharma and Lundbeck. Emma Cheesman-Ungstrup holds a 2017 - 2017 Københavns Universitet - University Of Copenhagen. With a robust skill set that includes Pharmaceutical Industry, Clinical Development, Drug Development, Regulatory Submissions, Biotechnology and more, Emma Cheesman-Ungstrup contributes valuable insights to the industry. Emma Cheesman-Ungstrup has 1 email on RocketReach.
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