Damon Daulerio

Director, Regulatory Affairs

For over 16 years Damon Daulerio worked in different jobs. Recently, this expert worked as a Director, Regulatory Affairs in Neos Therapeutics widening experience. This expert graduated from Fairfield University in 2002 where this professional got all the skills and knowledge. You can find this person in Dallas, Texas, where he is located nowadays. SoftwareOfficial has all the personal info you need to contact Damon Daulerio, such as this professional's phone number or email address. Send the request to get more info.
Name variants:
Damon Daulerio
Last updated Apr 30, 2024

Contact Information

Last Update
Jan 29, 2016
Location
Dallas, TX

Workplace

Neos Therapeutics
Director, Regulatory Affairs

Industry

Pharmaceuticals

Work History

Director, Regulatory Affairs

from Jun 2013

Associate Director, DRA

Aug 2005 — Jun 2013

Senior Regulatory Associate

Jan 2003 — Aug 2005

Regulatory Associate

Aug 1996 — Dec 2002

Education

1998 — 2002
1992 — 1996

Occupations

Executive
Director
Deputy Director
Operations Manager
Deputy Manager
Chief Executive

Skills

Pharmaceutical Industry
Regulatory Submissions
Clinical Development
Regulatory Affairs
Clinical Trials
GCP
Drug Development
FDA
Regulatory Requirements
Therapeutic Areas
Biotechnology
CTMS
Pharmaceutics

FAQs about Damon Daulerio

What is the main profession of Damon Daulerio?

The expert is a Director, Regulatory Affairs.

What are the profession of This professional?

These person's professions are Executive and Director

Where does Damon Daulerio currently live?

The professional currently lives in Dallas, Texas.

How many companies did Damon Daulerio work at?

Damon Daulerio worked at four jobs.

What education does Damon Daulerio have?

Damon studied at the Fairfield University from 1998 to 2002.

What is professional industry that Damon Daulerio worked in?

This person works in Pharmaceuticals industry.

Are there any professional skills, that Damon Daulerio has?

This professional has such skills as Pharmaceutical Industry, Regulatory Submissions, Clinical Development, Regulatory Affairs, Clinical Trials, GCP, Drug Development, and FDA.
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