Eva Maare's Location
Søborg, DK
Eva Maare's Work
- Senior Director QA GCP and Pharmacovigilance @ Genmab
- Head of Global Quality Audits, Senior manager @ LEO Pharma
- Director of GCP and PV Audits, Quality @ Novo Nordisk
- Head of ClinOps, Global Development Novo Nordisk @ Novo Nordisk
- Clinical Project manager @ Novo Nordisk
- International Trial Manager @ Novo Nordisk
- Faglig konsulent @ Fagforeningen Pharmadanmark
- Clinical Trial Manager and Validation Regulatory Affairs @ Dako
- Academic Coordinator and professionel @ Lægemiddelstyrelsen (Danish Medicines Agency)
- Head of Cytotoxic Department and Clinical Pharmacist @ Centralapoteket Københavns Amt
Eva Maare's Education
- Danmarks Farmaceutiske Universitet
MSc (Pharmacy)
1990 - 1996 - Engineering College of Copenhagen
Diploma (Project management)
2006 - 2010 - CBS E
Managing Medical Product Innovation MMPI/SIMI
2013 - 2014
Eva Maare's Skills
- Clinical Trials
- Clinical Development
- Clinical Research
- GCP
- Clinical Operations
- Pharmaceutical Industry
- CRO
- ICH-GCP
- Drug Development
- CTMS
Eva Maare's Summary
Eva Maare, based in Søborg, DK, is currently a Senior Director QA GCP and Pharmacovigilance at Genmab, bringing experience from previous roles at LEO Pharma and Novo Nordisk. Eva Maare holds a 1990 - 1996 MSc in Pharmacy @ Danmarks Farmaceutiske Universitet. With a robust skill set that includes Clinical Trials, Clinical Development, Clinical Research, GCP, Clinical Operations and more, Eva Maare contributes valuable insights to the industry. Eva Maare has 1 email on RocketReach.
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