
Mette Krøger Hare
Nutritionist

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About me
Manager, Safety Medical Writing at Novo Nordisk
Education

Department of Human Nutrition/Clinical Nutrition, Faculty of Life Sciences, University of Copenhagen
2009 - 2011M.Sc. Clinical Nutrition
Suhr's University College
2005 - 2009Prof. Bach Nutrition and Health - Human NutritionWith electives in: Food, Culture & HealthWeightloss Management & Coaching Additional Biochemistry and Statistics
Experience

Ebeltoft Kurcenter - Kurcenter Danmark
May 2008 - Sept 2008NutritionistResponsible for lectures in food and health. Counselling of people struggling with obesity and with a high prevalence of diabetes, hypertension, and hyperlipidaemia.

Ebeltoft Kurcenter - Kurcenter Danmark
Jan 2009 - Jan 2009LecturerLecturer on the subject Health and Nutrition in a collaboration between Kurcenter Danmark and Arriva.

Nestlé Nordic - Corporate Communication and Marketing Development
Aug 2010 - Aug 2012Strategic and communicational work to strengthen the Nutrition, Health and Wellness portfolio at Nestlé. - Giving lectures in nutrition and health to Nestlé employees- Performing nutritional assessments of products, and provide assessment on how to optimize nutritional value in products- Launching Nutrition, Health & Wellness initiatives at Nordic level- Producing communication material on nutrition- Article writing for internal magazine- Board member of Nestlé running club
Academic Employee
Jan 2012 - Aug 2012Nutritionist Student Worker
Aug 2010 - Jan 2012

Department of Human Nutrition/Clinical Nutrition, Faculty of Life Sciences, University of Copenhagen
Sept 2010 - Feb 2011Scientific AssistantScientific Assistant at a PhD project involving malnourished patients at Rigshospitalet. - Data collection- Diet counselling

Novo Nordisk
Sept 2012 - now- Clinical submission team lead (responsible for coordinating and leading the clinical documentation required for the NDA/MAA)- Heavily experienced with authority interactions, including Q&A as well as meeting packages/briefing documents and subsequent presentations - both for EMA, US FDA and PMDA. Especially proud of a type A meeting package for concizumab when the development was placed on clinical hold (phase 3a was subsequently reinitiated)- Experienced in writing several documents within the CTD structure, including clinical overview, summary of clinical safety and summary of clinical efficacy. - Subject matter expertise in the paediatric investigation plan/pediatric study plan (SOP author)- Trained in leader communication- Acting mentor Show less Three 8-month rotations in a talent development programme.The purpose of the programme was to attract and recruit young talent in order to strengthen the pipeline of potential future managers and specialists within Novo Nordisk.Employed in the clinical reporting track, my work focused mainly on medical writing in terms of ensuring efficient communication of the clinical trial results to regulatory authorities and the scientific community. In addition to this, I worked as a global scientific advisor within the area of medical affairs. In this position, I also worked with publication planning.1. Clinical Reporting, Soeborg, Denmark (Sep-2012 to May-2013)Main areas of work were within the GLP-1 receptor agonists portfolio and included publications (manuscripts, posters, abstracts), clinical trial reports and paediatric investigation plans.2. Strategic Scientific Communication, Princeton, New Jersey (May-2013 to Dec-2013)Worked with medical writing in the North American affiliate, Novo Nordisk Inc.Main areas of work were within the obesity trials (Phase 3a) and inflammation trials (Phase 1 and 2) and included working with publications (manuscripts, posters, abstracts), clinical trial reports and publication planning3. Global Medical Affairs, Søborg, Denmark (Jan-2014 to Sep-2014)Worked within the area of GLP-1 receptor agonists. Main area of work was scientific communication in relation to post-marketing activities for liraglutide 1.8 mg (management of diabetes), as well as pre-launch activities for liraglutide 3.0 mg (management of obesity). Key deliverables: External results meetings, global scientific expert meetings, publication planning, advisory boards, and internal scientific training. Show less
Manager, Safety Medical Writing at Novo Nordisk
Oct 2023 - nowSafety Surveillance Specialist
Sept 2023 - Oct 2023Senior Safety Surveillance Adviser
Mar 2021 - Sept 2023Senior Medical Writer
Mar 2018 - Mar 2021Medical Writer
Sept 2014 - Mar 2018Clinical Reporting Graduate
Sept 2012 - Aug 2014
Licenses & Certifications

GCP certified
Languages
- enEnglish
- daDanish
- swSwedish
- noNorwegian
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