Expert In Drug Development
Freelance
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Catherine Mathis Email & Phone Number
Expert in drug development
at
Freelance
1 work email found
@transgene.fr
LinkedIn matched
✓ Verified August 2026
4 data sources
Profile completeness 100%
Who is Catherine Mathis? Overview
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Quick answer
Catherine Mathis is listed as Expert in drug development at Freelance, based in Paris, ÎLe-De-France, France. AeroLeads shows a work email signal at transgene.fr and a matched LinkedIn profile for Catherine Mathis.
Catherine Mathis previously worked as Chief Development Officer at Coave Therapeutics and Vice President, Head of Regulatory Affairs at Coave Therapeutics. Catherine Mathis holds Master, Applied And Basic Toxicology from Université Paris Cité.
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Email format at Freelance
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{first}.{last}@transgene.fr
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Profile bio
About Catherine Mathis
Catherine Mathis is a Expert in drug development at Freelance. She possess expertise in clinical development, vaccines, biotechnology, clinical trials, clinical research and 10 more skills. Colleagues describe her as "Always prepared and cognizant of potential problems. Very calm personality; a delight to work with."
Listed skills include Clinical Development, Vaccines, Biotechnology, Clinical Trials, and 11 others.
Current workplace
Catherine Mathis's current company
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10 roles · 39 years
Catherine Mathis work experience
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Chief Development Officer
Current
Mar 2023 - Present
Vice President, Head Of Regulatory Affairs
CurrentCoave tx is a clinical stage biotechnology company focused on developing life changing gene therapies in rare ocular and CNS (Central Nervous System) diseases.Roles and Responsibilities: Determination and oversight of the regulatory strategy and operations supporting the advancement of Coave ’s programs.
Sep 2022 - Present
Chief Development Officer
Enterome is a clinical stage biopharmaceutical company developing first-in-class immunomodulatory drugs based on a unique ability to de-code the gut microbiome’s interaction with the immune system.Roles and Responsibilities: Supervision of pharmaceutical development, regulatory preclinical activities and regulatory affairs for Enterome products including peptides-based cancer vaccines and small molecules in oncology and GI diseases.
Mar 2019 - Sep 2022
Chief Operating Officer § Head Of Regulatory Affairs
Elsalysbiotech
Elsalys Biotech is a French biotechnology company dedicated to the development of therapeutic monoclonal antibodies in oncology and ophthalmic diseases.Roles and responsibilities: supervision of projects management activities and project managers team, management of alliance with pharma partners, in charge of products development activities up to first in man studies, interactions with regulatory bodies as needed.
Feb 2016 - Feb 2019
Senior Director, Regulatory Affairs In Drugs And Biologics
Roles and responsibilities: Advice of pharma and biotech companies in product development for Europe and the USA for biologics/innovative products in association or not with companion diagnostic assays for the purpose of the personalized medicine. Disease areas: oncology and infectious diseases.
Nov 2014 - Dec 2015
Senior Director, Head Of Regulatory Affairs
Transgene is a publicly traded French biopharmaceutical company focused on discovering and developing targeted immunotherapies for the treatment of cancer and infectious diseases.Setting-up and Development of the Regulatory Affairs Department of Transgene Headquarter- Supervision of regulatory team with ability to manage several levels of expertise - Supervision of worldwide regulatory activities for development of Transgene gene therapy products with development of companion diagnostic test (CDx) - Participation to due diligences for licensing-in and licensing-out activities- Interaction with partners: alignment of regulatory strategy, management of regulatory operational aspects, member of Joint Steering Committees- Early interaction with Health Technology Assessment (HTA) Agencies for market access preparation in collaboration with the marketing/business and medical departments.Member of internal steering committees.Up to 2007: supervision of preclinical safety assessment activities
Feb 2000 - Oct 2014
Regulatory Affairs Manager And Head Of Regulatory Preclinical Toxicology
1994 - 2000
~6 yrs
Clinical Research Monitor
1989 - 1994
~5 yrs
Clinical Research Assistant
1988 - 1989
~1 yr
2 education records
Catherine Mathis education
Master, Applied And Basic Toxicology
Université Paris Cité
Pharm D, Pharmacy
Université Paris Cité
FAQ
Frequently asked questions about Catherine Mathis
Quick answers generated from the profile data available on this page.
What company does Catherine Mathis work for?
Catherine Mathis works for Freelance.
What is Catherine Mathis's role at Freelance?
Catherine Mathis is listed as Expert in drug development at Freelance.
What is Catherine Mathis's email address?
AeroLeads has found 1 work email signal at @transgene.fr for Catherine Mathis at Freelance.
Where is Catherine Mathis based?
Catherine Mathis is based in Paris, ÎLe-De-France, France while working with Freelance.
What companies has Catherine Mathis worked for?
Catherine Mathis has worked for Freelance, Coave Therapeutics, Enterome, Elsalysbiotech, and Voisin Consulting Life Sciences.
How can I contact Catherine Mathis?
You can use AeroLeads to view verified contact signals for Catherine Mathis at Freelance, including work email, phone, and LinkedIn data when available.
What schools did Catherine Mathis attend?
Catherine Mathis holds Master, Applied And Basic Toxicology from Université Paris Cité.
What skills is Catherine Mathis known for?
Catherine Mathis is listed with skills including Clinical Development, Vaccines, Biotechnology, Clinical Trials, Clinical Research, Toxicology, Biopharmaceuticals, and Life Sciences.
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