Richard Mountfield

Senior Vice President, Regulatory Affairs and Quality

With work experience over 23 years, this professional is nowadays working at Constellation Pharmaceuticals situated in 518 as a Senior Vice President, Regulatory Affairs and Quality. Richard received his education from 1990 to 1993 at the Aberystwyth University. Richard Mountfield lives in Bethel, Connecticut. To contact Richard, you can search for their phone number or e-mail or receive additional information by requesting access to this person's further details on this webpage.
Name variants:
Dick Mountfield, Rick Mountfield, Ricky Mountfield, Rich Mountfield, Richie Mountfield
Last updated Jun 05, 2024

Contact Information

Last Update
Jul 1, 2022
Email
rm**@rdg.boehringer-ingelheim.com, rm**@gmail.com
Location
Bethel, CT

Workplace

Constellation Pharmaceuticals
Senior Vice President, Regulatory Affairs and Quality

Cambridge, MA

Industry

Pharmaceuticals, Mfg Pharmaceutical Preparations

Work History

Senior Vice President, Regulatory Affairs and Quality

215 1St St, Cambridge, MA 02142
from Jul 2020

Senior Vice President, Regulatory Affairs and Drug Development

55 Cambridge Pkwy SUITE 400, Cambridge, MA 02142
from Jun 2018

Vice President, Head of Regulatory Affairs and Pharmacovigilance

55 Cambridge Pkwy SUITE 400, Cambridge, MA 02142
from Oct 2016

Vice President, Global Head of Regulatory Affairs and Clinical Operations

Feb 2016 — Aug 2016

Senior Director, Oncology Drug Regulatory Affairs - Oncology Global Development

May 2013 — Feb 2016

Senior Director, Oncology Drug Regulatory Affairs - Early Development

Regulatory global lead responsible for developing and driving global regulatory strategies for early oncology programs, including the evaluation of regulatory risks/gaps and developing regul...
Apr 2012 — Apr 2013

Director, Drug Regulatory Affairs - Novartis Institutes For Biomedical Research

Regulatory global lead responsible for developing and driving global regulatory strategies for early oncology programs, including the evaluation of regulatory risks/gaps and developing regul...
Jul 1, 2010 — Mar 1, 2012

Senior Associate Director, Drug Regulatory Affairs

Apr 2001 — Jul 2010

Laboratory Head, Drug Discovery

Major responsibility included representation of DMPK on Discovery research teams. Coordinated and managed in vitro drug metabolism studies and in vivo pharmacokinetic experiments using appro...
Sep 1999 — Mar 2001

Senior Scientist, Drug Development

Managed a number of scientists investigating the metabolism of NCEs and pharmaceutical proteins, functioning in the role of both Drug Development and Drug Discovery support, including precli...
Dec 1995 — Aug 1999

Team Leader

Hls
Managed a group of scientists investigating the metabolism/biotransformation of radiolabeled NCEs in a number of test systems. This involved conducting ADME studies utilizing pertinent techn...
Oct 1993 — Dec 1995

Manager

For more than 130 years, Boehringer Ingelheim has been committed to the research, development, and manufacturing of new medications with high therapeutic value for people and animals. As a f...

Occupations

Executive
Manager
Operations Manager

Skills

Drug Development
Regulatory Submissions
Clinical Development
Regulatory Affairs
Pharmaceutical Industry
Oncology
Clinical Trials
Drug Discovery
Pharmacokinetics
Fda
Clinical Research
Regulatory Requirements
R&D
Strategy
Drug Metabolism
Life Sciences
Adme
Immunology
Regulatory Strategy
Preclinical Development
Influencing
Lifesciences
Dmpk
Regulatory Risk
Global Drug Development
Global Regulatory Submissions
Clini
Clinic
Sop Development
U.s. Food and Drug Administration
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