Linda Thurmond Keelan

Retired- Vp, Drug Safety and Pharmacovigilance

Linda Thurmond Keelan is a high-level expert, who works in New Haven Pharmaceuticals, Inc main office of which is in 315. on the position of Retired- Vp, Drug Safety and Pharmacovigilance from 2016. This person has earned professional experience in more than eight positions at various companies. Linda Thurmond Keelan went to the Headland High School, East Point, Ga and received education. Atlanta, Georgia is the city, where this professional was lastly known to settle. The professional's email address and phone can be easily accessed through this website on demand.
Name variants:
Lynda Keelan, Lindy Keelan, Lin Keelan, Lynn Keelan, Lynne Keelan
Last updated Jun 02, 2024

Contact Information

Last Update
Jul 13, 2022
Email
lj**@comcast.net
Location
Atlanta, GA
Company
New Haven Pharmaceuticals, Inc.

Workplace

Retired- Vp, Drug Safety and Pharmacovigilance

Work History

Retired- Vp, Drug Safety and Pharmacovigilance

116 Washington Ave, North Haven, CT 06473
from Jan 2016

Senior Director, Drug Safety and Medical Information

444 south Ellis Rd, Chandler, AZ
Feb 1, 2012 — Dec 2015

Associate Director, Drug Safety

Jan 2011 — Jul 2011

Director, Medical Affairs

300 Campus Dr, Florham Park, NJ 07932
Dec 1993 — Aug 2010

Senior Mngr, Medical Information

2001 — 2003

Drug Safety Associate

1999 — 2001

Medical Coordinator

Designee to the Medical Diretor for RA, QA, AEs, and Medical Information.
1993 — 1999

Senior Account Executive, National Accounts

Sold health, life, STD, LTD & Key Man Insurance to groups of &gt 1,000 based in Washington DC. Maintained a block of business with annual premiums totalling &gt 35m. Licensed in DC, MD & ...
Mar 1978 — Dec 1991

Occupations

Executive
Vice President
Senior Director
Chief Executive
Senior Manager
Operations Manager

Skills

Pharmaceutical Industry
Pharmacovigilance
Drug Safety
Medical Affairs
Oncology
Medical Writing
Clinical Development
Fda
Gcp
Healthcare
Pharmaceutical Sales
Biotechnology
Medical Devices
Cardiology
Clinical Trials
Sop
Neurology
Diabetes
Medicine
Managed Care
Microsoft Office
Quality Assurance
Regulatory Affairs
Product Launch
Software Documentation
Life Sciences
Gastroenterology
Regulatory Submissions
Endocrinology
Clinical Research
Good Clinical Practice
Validation
Therapeutic Areas
Cro
Lifesciences
Infectious Diseases
Standard Operating Procedure
Pharmaceuticals
Documentation
Psychiatry
U.s. Food and Drug Administration
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