Welcome to Dr. Gloria's freelance profile!
This freelancer is available part-time (4 days per week) but hasn't confirmed their availability in over 7 days.
Part-time, 4 days per week
Location and workplace preferences
- Location
- Lucerne, Switzerland
- Remote only
- Primarily works remotely
Preferences
- Project length
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- ≤ 1 week
- ≤ 1 month
- Between 1-3 months
- Business sector
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- Biotech
- Research
- Retail (Small Business)
- Publishing
- Education & E-learning
+6 autres
Verifications
Freelancer code of conduct signed
Read the Malt code of conduct
Languages
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English
Fluent
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German
Fluent
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Spanish
Native or bilingual
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Catalan
Native or bilingual
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French
Basic
Categories
Skills (16)
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Beginner Intermediate Advanced
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Beginner Intermediate Advanced
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Beginner Intermediate Advanced
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Beginner Intermediate Advanced
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Beginner Intermediate Advanced
Dr. Gloria in a few words
Selection of services
- Product development: Technical consulting, Idea discussion, Product design, Market research, Regulatory compliance, Feasibility study
- Technical, Scientific & Medical Writing: White paper, Journal article, Review article, Blog article, News article, Regulatory documents, Clinical trial documents, Marketing content, Educational content
- Data science & analysis: Product design & development, Data processing
- Academic research: Qualitative research, Internet research, Systematic reviews and meta-analysis, Review article, Evidence-based answers, Secondary data compilation, Literature search
CV
15 years of scientific experience, holding a valuable expertise in Project management and scientific writing.
• Progressed from fundamental multidisciplinary research (Chemistry, Nanobiotech, Biochemistry) to in vitro Pharmacology (Cell Biology, Target ID, Proteomics), moving to Pharmaceutical R&D (ADME/DMPK) and getting into Project Management and Clinical trial OP, with a last immersion into the Medical Device Development.
• This has provided me with a deep knowledge in a variety of scientific and clinical fields, as well as a broad understanding of the drug development process from bench to market and beyond.
• My fluency in four languages (English, German, Spanish, Catalan) combined with my international career (Spain, Germany, Switzerland) in multicultural environments allows me to write for a diversity of public.
Experience
VeNaV Consulting
Research
Director - As a freelancer
IVAG
Medical
Scientist & Regulatory affairs
Merck KGaA - Merck KGaA
Pharmaceuticals industry
Project Representative
- Medical & Regulatory writing. Data analysis and management. Preparation/review of regulatory documents and templates.
- Clinical research. Clinical trial operations. Bioanalysis and Drug Metabolism. Sample logistics
- Preclinical research. Method development. Mechanistic insights into complex drug behaviours.
Max Plank Institut
Research
Scientist in Pharmacology
- Academic research: Execution of 4 projects, involving organization of cross-functional teams. Research: mode-of-action of small bioactive molecules, development of ex-vivo target validation assays.
CSIC Barcelona
Chemical
PhD Fellow in Drug Discovery
- Multi-tasking in inter-institutional projects, including task coordination.
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Education
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PhD in Science, Chemistry
University of Barcelona
2011 Drug Discovery, Biotechnology, Biochemistry, Medicinal Chemistry
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Master in Science
University of Barcelona
2008 Medicinal Chemistry, Biotechnology, Neuroscience
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Licenciature, Bachelor in Chemistry
Autonomous University of Barcelona
2006