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Dr. Gloria V.DG

Dr. Gloria V.

Project Manager, Technical Writing, career coacher

On-demand
Lucerne, CH
8-15 years

Average response time: 1 hour

About Dr. Gloria

Consultant with 15 years of multidisciplinary scientific experience, holding a valuable expertise in Project Management, Scientific Writing & pre-Clinical/Clinical R&D.

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.
  • English

    Fluent

  • German

    Fluent

  • Spanish

    Native or bilingual

  • Catalan

    Native or bilingual

  • French

    Basic

Remote only
Primarily works remotely

Experience

  • VeNaV Consulting
    Director
    RESEARCH
    June 2021 - Today (5 years)
    Zúrich, Switzerland
    Project Management, Scientific Writing & pre-Clinical/Clinical R&D
  • IVAG
    Scientist & Regulatory affairs
    MEDICAL
    December 2019 - May 2021 (1 year and 6 months)
    Project representation. Medical writing. Regulatory affairs. Monitoring of clinical and pre-clinical activities. Supervision of pre-clinical studies. Data management. Optimization of processes.
  • Merck KGaA
    Project Representative
    PHARMACEUTICALS INDUSTRY
    January 2016 - November 2019 (3 years and 11 months)
    Darmstadt, Germany
    - Project Management. Monitoring and outsourcing.
    - 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.

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Education

  • PhD in Science, Chemistry
    University of Barcelona
    2011
    Drug Discovery, Biotechnology, Biochemistry, Medicinal Chemistry
  • Master in Science
    University of Barcelona
    2008
    Medicinal Chemistry, Biotechnology, Neuroscience

Skill set (16)

Categories