About Sandrine
- Rapid and high-quality scientific and medical writing (e.g., protocols, study reports, scientific articles);
- Design, execution, and analysis of usability studies;
- In-depth literature reviews and synthesis;
- Preparation of scientific communication materials and deliverables.
French
Native or bilingual
English
Fluent
German
Basic
Experience
- GeNeuroPreclinical Study ManagerPHARMACEUTICALS INDUSTRYJanuary 2015 - April 2020 (5 years and 3 months)Preclinical studies manager: Toxicology and Safety Pharmacology studies, Development of preclinical In vivo and In vitro models, Clinical team support (IB, study design, SAP), Scientific communication (conferences and articles) CROs management, technicians supervision. Therapeutic area: Type 1 Diabètes, Metabolic disorders and Multiple Sclerosis,
- 2025 - Becton Dickinson FR EMEA - Europe Holdings SAS (EUR)Clinical and Human Factor ScientistPHARMACEUTICALS INDUSTRYApril 2020 - May 2025 (5 years and 1 month)Le Pont-de-Claix, FranceManagement of usability studies to support Medical Device development (study design, conduction, analysis, report), Literature review, Risk Management, Customer and business support.
- OHSU | Oregon Health & Science UniversityPostdoctoral ResearcherMarch 2014 - October 2014 (7 months)Design of in vivo studies, Single cell RNA-seq (C1 Fluidigm, libraries prep), flow cytometry, histology, stereomicroscopy, molecular biology (CRISPR/ Cas9).
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Education
- Ingénieur, BiosciencesINSA Lyon2010Ingénieur, Biosciences
- Doctor of Philosophy (PhD), Cellular BiologyUniversité Joseph Fourier (Grenoble I)2013Doctor of Philosophy (PhD), Cellular Biology
Skill set
Categories
- Other