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Marie Parrish Email & Phone Number
Senior Director, CMC Regulatory Strategy
at
Roivant Sciences
1 work email found
@roivant.com
1 phone found area 908
LinkedIn matched
✓ Verified Jun 2026
4 data sources
Profile completeness 100%
Current company
Role
Senior Director, CMC Regulatory Strategy
Location
New York, New York, United States
Who is Marie Parrish? Overview
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Quick answer
Marie Parrish is listed as Senior Director, CMC Regulatory Strategy at Roivant Sciences, based in New York, New York, United States. AeroLeads shows a work email signal at roivant.com, phone signal with area code 908, and a matched LinkedIn profile for Marie Parrish.
Marie Parrish previously worked as Senior Director Regulatory CMC Strategy at Roivant Sciences and CMC Topic Group Chair at Iriss Forum (Iriss-Forum.Org). Marie Parrish holds Ph.D, Pharmaceutical Analysis from Rutgers University.
Company email context
Email format at Roivant Sciences
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{first}.{last}@roivant.com
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Profile bio
About Marie Parrish
Accomplished regulatory professional and experienced manager with cross-functional expertise in all phases of drug development (Phase I through post NDA). Extensive background in global CMC submission requirements, quality and cGMP issues. Experience with small and large molecule registration submissions. Excellent interpersonal skills and a strong scientific foundation.Specialties: CMC content for world-wide regulatory submissions - clinical phase through registration for both small and large molecules; drug development; analytical development activities
Listed skills include Regulatory Submissions, Gmp, Drug Development, Fda, and 39 others.
Current workplace
Marie Parrish's current company
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12 roles
Marie Parrish work experience
A career timeline built from the work history available for this profile.
Sep 2021 - Present
Cmc Topic Group Chair
Sep 2017 - Jan 2023
Director, Regulatory Affairs, Strategy
Jan 2020 - Aug 2021
Director Of Regulatory Affairs -Innovative Pharmaceuticals
Accountable for the development and implementation of regulatory strategy to support clinical trials and product registration
Nov 2016 - Dec 2019
Associate Director, Manufacturing Technology Cmc Regulatory Support
Responsible for the CMC technical content for US, EU, JP submissions from clinical phase through registration submission for new molecular entities (NMEs). I continue to be an active member of the e-CTD CMC Industry Working Group.
Dec 2012 - Nov 2016
Associate Director, Cmc Dossier Coordination
I led the US team who were responsible for the CMC technical content for global submissions from clinical phase through registration submission. I have experience with Agency interactions (FDA) and am an active member of the e-CTD CMC Industry Working Group.
Jan 2007 - Mar 2012
Assistant Director, Cmc Dossier Coordination
CMC content for world-wide regulatory submissions - clinical phase through registration; Lead Bridgewater team
Jan 2005 - Dec 2006
Manager, Cmc Documentation
- Ensure scientific consistency, check global regulatory compliance and ensure timely availability of CMC documentation (including answers to questions from regulatory authorities) coming from An. Sc., Ph. Sc., Chemical.
- Provide a departmental regulatory support to the authors of CMC documents in CMC, based on business requirements and on a high technical experience
- Compile the CMC dossier and write the technical/scientific storyline
- Contribute to the creation and update of templates for CMC documentation
- Supervise 3 scientists in NJ
Jul 2004 - Dec 2004
Cmc Documentation Project Leader
- Ensure scientific consistency, check global regulatory compliance and ensure timely availability of CMC documentation (including answers to questions from regulatory authorities) coming from An. Sc., Ph. Sc., Chemical.
- Provide a departmental regulatory support to the authors of CMC documents in CMC, based on business requirements and on a high technical experience
- Compile the CMC dossier and write the technical/scientific storyline
Mar 2001 - Jun 2004
Research Investigator
I was a team leader of a multidisciplinary group involved in developing prototype formulations for commercial development.
Jun 2000 - Mar 2001
Research Investigator
- I was part of Parke-Davis R&D division of Warner LambertResearch Associate Aug 1995 to March 2001Senior Scientist May 1994 to July 1995Scientist June 1992 to April 1994
- Independently coordinated and performed transfer of analytical methodologies to Ireland site including the completion of all required documentation.
- Serve as analytical project team representative for new drug product candidates.
- Analytical Representative for international pre-approval inspection team that resulted in successful PAI.
- Coordinate testing, documentation, and method changes with Quality Control departments for drug products.
- Coordinate analytical work required for compounds in Phase I - IV to ensure on time testing/reporting of results to support regulatory filings.
Jun 1992 - Jun 2000
2 education records
Marie Parrish education
Ph.D, Pharmaceutical Analysis
Rutgers University
B.S., Chemistry
University Of The Sciences In Philadelphia
FAQ
Frequently asked questions about Marie Parrish
Quick answers generated from the profile data available on this page.
What company does Marie Parrish work for?
Marie Parrish works for Roivant Sciences.
What is Marie Parrish's role at Roivant Sciences?
Marie Parrish is listed as Senior Director, CMC Regulatory Strategy at Roivant Sciences.
What is Marie Parrish's email address?
AeroLeads has found 1 work email signal at @roivant.com for Marie Parrish at Roivant Sciences.
What is Marie Parrish's phone number?
AeroLeads has found 1 phone signal(s) with area code 908 for Marie Parrish at Roivant Sciences.
Where is Marie Parrish based?
Marie Parrish is based in New York, New York, United States while working with Roivant Sciences.
What companies has Marie Parrish worked for?
Marie Parrish has worked for Roivant Sciences, Iriss Forum (Iriss-Forum.Org), Sun Pharma Advanced Research Company Ltd., Glenmark Pharmaceuticals, and Imclone Systems, A Wholly-Owned Subsidiary Of Eli Lilly And Company.
How can I contact Marie Parrish?
You can use AeroLeads to view verified contact signals for Marie Parrish at Roivant Sciences, including work email, phone, and LinkedIn data when available.
What schools did Marie Parrish attend?
Marie Parrish holds Ph.D, Pharmaceutical Analysis from Rutgers University.
What skills is Marie Parrish known for?
Marie Parrish is listed with skills including Regulatory Submissions, Gmp, Drug Development, Fda, Pharmaceutical Industry, Formulation, Ind, and Cmc.
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