Cheryl Madsen

Vice President Regulatory Affairs

With work experience over 38 years, this person is nowadays working at Calithera Biosciences that is based in 1092 as a Vice President Regulatory Affairs. Cheryl received his education from 1994 to 1998 at the University of California, Berkeley. This expert has earned certifications in Global Rac (Certification) This expert lives in Sharp Park, California. To contact directly Cheryl, you can look for their phone or e-mail address or find further info by requesting access to the person's further details on SoftwareOfficial.
Name variants:
Cherie Madsen, Cheri Madsen
Last updated Jul 05, 2024

Contact Information

Last Update
Jul 14, 2022
Email
cm**@pdl.com, ma**@yahoo.com
Location
Sharp Park, CA

Workplace

Vice President Regulatory Affairs

South San Francisco, CA

Industry

Pharmaceuticals, Commercial Physical Research

Work History

Vice President Regulatory Affairs

343 Oyster Point Blvd SUITE 200, South San Francisco, CA 94080
from Sep 2019

Vice President Regulatory Affairs

from Sep 2017

Project Team Leader, Xtandiã Â

235 east 42Nd St, New York, NY 10036
With a deep understanding of disease biology, global drug development and commercialization, effectively provide direction and leadership to the cross-functional Project Team for Xtandi and ...
Apr 2015 — Mar 2016

Senior Director, Regulatory Affairs

Apr 2012 — Sep 2017

Director, Regulatory Affairs and Compliance

2910 7Th St, Berkeley, CA 94710
Jun 2010 — Apr 2012

Associate Director, Regulatory Affairs, Oncology

Led the BLA/MAA filing team for zalutumumab (HuMax-EGFr) in squamous cell carcinoma of the head and neck which included managing a cross-functional team of 50+ employees, providing executiv...
May 2007 — Mar 2010

Director, Regulatory Affairs

Directed the regulatory strategy and development of Asentar™ (DN-101) in both the US and EU; exploring the potential for EU conditional approval for the treatment of androgen independent pr...
Mar 2006 — Apr 2007

Associate Director, Regulatory Affairs

Directed the regulatory strategy and development of Nuvion® (visilizumab), an anti-CD3 monoclonal antibody fast-tracked for the treatment of ulcerative colitis and Crohn’s Disease. Interac...
Dec 2004 — Mar 2006

Senior Manager, Regulatory Affairs

1 Dna Way, South San Francisco, CA 94080
Feb 1992 — Dec 2004

Senior Manager, Regulatory Affairs

1 Dna Way, South San Francisco, CA 94080
1992 — 2004

Assoc Director, Regulatory Affairs

Education

Occupations

Executive
Deputy Director
Senior Manager
Scientist
Biotechnology Professional
Deputy Manager
Chief Executive
Operations Manager
Biologist
Biological Scientist

Skills

Regulatory Requirements
Regulatory Affairs
Drug Development
Biotechnology
Clinical Development
Clinical Trials
Strategy
Oncology
Regulatory Analysis
Fda
Pharmaceutical Industry
Biopharmaceuticals
Regulatory Submissions
Ind
Life Sciences
Biologics
Drug Discovery
Gmp
Pharmacovigilance
Cell
Nda
Ectd
Regulatory Strategy
Change Control
Lifesciences
Monoclonal Antibodies
Program Management
R

FAQs about Cheryl Madsen

What's the main profession of Cheryl Madsen?

The expert is a Vice President Regulatory Affairs.

What are the main profession of The professional?

These person's professions are Executive and Deputy Director

Where is Cheryl Madsen located?

Cheryl Madsen is located in Sharp Park, California.

What is the professional's email?

The professional's email is cm**@pdl.com and ma**@yahoo.com.

Where did Cheryl Madsen work?

The professional worked at Calithera Biosciences, Peloton Therapeutics Now A Part of Merck & Co.

What education does Cheryl Madsen have?

Cheryl studied at the University of California, Berkeley from 1994 to 1998.

Are there any professional certifications Cheryl Madsen has?

This expert received the following certifications: Global Rac (Certification).

Are there any special industries Cheryl Madsen works in?

This person works in Pharmaceuticals industry.
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