Charlotte Dubé

Principal Scientist, Preclinical Nonclinical & Clinical Studies @Providence Therapeutics

Québec, QC, CA
MOBILE NUMBERS
+91 *********19

Signup · Get unlimited contacts

WORK HISTORY

Feb 2023 — Present

Principal Scientist, Preclinical Nonclinical & Clinical Studies @Providence Therapeutics

View department →

Québec, CA

EDUCATION

2007 — 2008

Université Laval

Short program in pharmaceutical development, Développement pharmaceutique

1996 — 1999

Université de Sherbrooke

Bachelor's Degree, Microbiology

2000 — 2005

Université Laval

Ph.D. Degree, Physiology

SKILLS

Utilisation De Bioequiv, Pks (Pharsight Knowledgebase Server), Pks ReporterWinnonlin, Autopilot, Sas;Suite OfficeGénomique Et Biologie MoléculaireTransfection De Cellules Au Phosphate De CalciumEssais EnzymatiquesCulture Cellulaire Et BactérienneCytométrie En Flux (Facs)Mutagénèse DirigéeExtraction D’arnEssai À Retardement Sur Gel (Emsa)Outils De Protéomique : Sds-Page En 1d Et 2dWestern BlottingExtraction De Protéines, ImmunoprécipitationImmunohistochimie Et ImmunofluorescenceMicroscopie Électronique À Balayage Et À TransmissionSupervision D'étudiants Gradués Et Stagiaires

ABOUT CHARLOTTE DUBÉ

Senior scientist with over 18 years of experience in the research and biopharmaceutical industry, experience working in a CRO and as the sponsor. PhD in sciences. Project and team management. Highly efficient, quality and detail-oriented with strong ability working both independently and collaboratively in a team environment or with external stakeholders. Strong organizational and communication skills. Ability to work in high stress contexts with tight deadlines.More than 12 years in product development with expertise in vaccine preclinical development (mRNA and virus-like particles (VLP) vaccines targeting infectious diseases and cancer, early and late-phase preclinical programs). Contributed to the preclinical development of COVIFENZ®, a SARS-CoV-2 vaccine later approved by Health Canada. Experience in cancer patient trial management, oversight and documentation. Six (6) years as PK scientist in a CRO carrying out clinical studies (especially bioequivalence).

This profile is compiled from publicly available professional sources. Unifers is not affiliated with or endorsed by LinkedIn. Request removal of this profile.