Skill set (16)
Dr. Gloria in a few words
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.
Experience
- VeNaV ConsultingDirectorRESEARCHJune 2021 - Today (3 years and 6 months)Zúrich, SuizaProject Management, Scientific Writing & pre-Clinical/Clinical R&D
- IVAGScientist & Regulatory affairsMEDICALDecember 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 KGaAProject RepresentativePHARMACEUTICALS INDUSTRYJanuary 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.
Recommendations
Education
- PhD in Science, ChemistryUniversity of Barcelona2011Drug Discovery, Biotechnology, Biochemistry, Medicinal Chemistry
- Master in ScienceUniversity of Barcelona2008Medicinal Chemistry, Biotechnology, Neuroscience
- Licenciature, Bachelor in ChemistryAutonomous University of Barcelona2006