Nathalie Rioux

Senior Director, Certara Strategic Consulting- Integrated Drug Development

We found the following information about Nathalie Rioux at Certara, where this expert has worked as a Senior Director, Certara Strategic Consulting- Integrated Drug Development since 2018. Nathalie's total work experience is over 18 years, during which time they had at least eight jobs at different places to develop professional skills. Nathalie studied at the Université Laval from 1996 to 2000. Nathalie Rioux is skilled in two languages: French and English. Nathalie Rioux can be found in Cambridge, Massachusetts – where this person currently lives. You can contact with Nathalie by searching for phone number or email or find further information by requesting access to this person's details.
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Natalie Rioux

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Contact Information

Last Update
Jul 11, 2022
Email
nr**@epizyme.com, th**@videotron.ca, na**@h3biomedicine.com
Location
Cambridge, MA
Company

Workplace

Certara
Senior Director, Certara Strategic Consulting- Integrated Drug Development

Princeton, NJ

Industry

Pharmaceuticals

Work History

Senior Director, Certara Strategic Consulting- Integrated Drug Development

Princeton, NJ
from Oct 2018

Head of Dmpk and Clinical Pharmacology

300 Technology Sq FLOOR 5, Cambridge, MA 02139
Built H3 DMPK and bioanalysis team. Drove strategic and tactical activities around ADME, PK, and bioanalysis across the discovery and development space. Contributed to regular reviews of p...
Sep 2015 — Oct 2018

Principal Scientist

400 Technology Sq, Cambridge, MA 02139
Represented DMPK on multidisciplinary discovery and preclinical programs including alliances with GSK (identification a potential first-in-class PRMT5 inhibitor), Eisai and Celgene. Partne...
May 2013 — Sep 2015

Senior Research Scientist

Head of the metabolism and excretion sub-group: coordinate and/or executed all related in vitro and in vivo assays. Managed and/or executed in vitro drug-drug interaction studies. Impleme...
2007 — Mar 2013

Manager Dmpk

Managed all internal activities related to preclinical drug metabolism studies, from study design elaboration to report redaction. Supervised one DMPK specialist and two analysts. Selecte...
2006 — 2007

Research Scientist In Vitro Dmpk

251 Ballardvale St, Wilmington, MA 01887
formerly CTBR) Served as a Study Director: responsible for the design, conduct and reporting of in vitro drug metabolism studies. Scientifically directed the Team Leader and all technical st...
2003 — 2006

Research Scientist

Executed and/or coordinated all activities of the group related to in vitro metabolism, solubility and permeability assays. Improved existing protocols and implemented new assays, as well ...
2002 — 2003

Post-Doctoral Fellow

Establishment of a sophisticated in vitro approach to metabolism studies of new pharmaceutical entities: application to the liver metabolism of nucleosides.
2000 — 2002

Education

1996 — 2000
1994 — 1996
1991 — 1994

Occupations

Executive
Senior Director
Project Manager
Senior Manager
Operations Manager
Project Managers

Skills

Drug Metabolism
Dmpk
In Vitro
Pharmacokinetics
Adme
Drug Discovery
Pharmaceutical Industry
Hplc
In Vivo
Glp
Assay Development
Bioanalysis
Pharmacodynamics
Cro
Project Management
Pharmacology
Metabolism
Drug Design
Gastroplus
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