I am searching for a job with stability and that treats its employees well. I would like it to be my last job. I am considering jobs in the CRO, biotechnology, pharmaceutical, government and academic industries.

COMPANY	POSITION HELD	DATES WORKED
University of Medicine and Health Sciences / St Eustatius School of Medicine	Associate Professor of Physiology and Pharmacology	2/2009 - 1/2010
(Confidential)	Consultant	7/1999 - Present
Otsuka	Senior Scientist IV	5/1996 - 6/1999
Texas Biotechnology	Clinical Project Manager, Medical Science Liaison, Pharmacologist, CRA	9/1992 - 2/1996
Glaxo	Research Scientist	5/1988 - 8/1992

SCHOOL	MAJOR	YEAR	DEGREE
University of Nebraska Medical Center	Cardiovascular Physiology	1986	Doctorate Degree
University of Kansas / Oral Roberts University	Aerospaced Engineering / Biology	1978	Bachelor Degree

TYPE	TITLE	URL	DESCRIPTION
Website	LinkedIn	media url	Networking site

Highlights:

* Part of a team which successfully got drugs approved under time and under budget * Wrote white papers, INDs, NDAs, ANDAs, 510(k)s, clinical study reports, protocols, investigator brochures * Business development: evaluated research projects, strategic planning, "go / no-go" decisions, licensing, data analysis * Travel award to Japan, International Microcircculation Society

Companies I like:

Quintiles, PRA, Glaxo, Amgen, Allergan, Genenteck, Biogen

Software Implementation
Requirements Analysis & Specification
Project Management
Medical and publication writing
Medical Science Liaison
Regulatory Affairs
Drug Discovery / Toxicology / PK/PD

• MSL
• Medical Writer
• Clinical Project Manager
• Drug Safety
• Pharmacologist
• Regulatory Affairs
• Medical Science Liaison
• Director of Clinical Research
• Regulatory Affairs Manager
• Compliance

Medical writing (publications and regulatory submissions), medical science liaison, clinical project manager (drugs and devices), regulatory affairs manager (drugs, biologics), pharmacologist and toxicologist