Cristiane Jensen's Location
Farum, DK
Cristiane Jensen's Work
- Clinical Supplies Trial Set-Up Professional @ Novo Nordisk
- Distance Learning Programme Tutor (Protocol Development) @ London School of Hygiene and Tropical Medicine, U. of London
- Principal Electronic Submissions Coordinator and Medical Writer @ Lundbeck
- Clinical Submission Coordinator @ Lundbeck
- Regulatory Affairs Associate @ Novo Nordisk
- Text Coordinator @ Novo Nordisk
- Research Associate @ Novozymes
- Medical Laboratory Technologist at Clinical Biochemical Lab. @ Amager og Hvidovre Hospital
- Pharmacist @ Public Health Agency of São Paulo VISA
- Biochemistry student at the medical laboratory @ paranaclinicas.com.br
Cristiane Jensen's Education
- London School of Hygiene and Tropical Medicine, U. of London
Master's degree (Clinical Trials)
2015 - 2022 - UnG Universidade de Guarulhos
(Pharmacy and Biochemistry continued)
2000 - 2001 - Pontifícia Universidade Católica do Paraná
Pharmacy and Biochemistry
1996 - 2000
Cristiane Jensen's Skills
- Pharmaceutical Industry
- Regulatory Affairs
- Regulatory Submissions
- Regulatory Operations
- Labelling
- Proofreading
- Documentum
- Clinical Development
- GCP
- Clinical Trials
Cristiane Jensen's Summary
Cristiane Jensen, based in Farum, DK, is currently a Clinical Supplies Trial Set-Up Professional at Novo Nordisk, bringing experience from previous roles at London School of Hygiene and Tropical Medicine, U. of London, Lundbeck and Novo Nordisk. Cristiane Jensen holds a 2015 - 2022 Master's degree in Clinical Trials @ London School of Hygiene and Tropical Medicine, U. of London. With a robust skill set that includes Pharmaceutical Industry, Regulatory Affairs, Regulatory Submissions, Regulatory Operations, Labelling and more, Cristiane Jensen contributes valuable insights to the industry. Cristiane Jensen has 2 emails on RocketReach.
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