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Experienced CRO management professional offering 20+ years of pharmaceutical toxicology experience
Looking for opportunities to excel in sponsor/CRO relationships. Last 10 years have been devoted to monitoring, managing, and building relationships with preclinical Contract Research Organizations (CROs) through demonstrated ability to plan, coordinate and interact professionally with all levels of staff both internally and externally. I possess excellent communication and interpersonal skills and have a firm understanding of toxicology and related science.
Life Scientist
About Me
Industry: |
Science & Biotech |
---|---|
Occupation: |
Life Scientist |
Highlights: |
Been promoted at every job role held in my 20+ years of toxicology, including a recent promotion in Dec 2007. |
Ideal Companies: |
Biotech or pharmacuetical companies |
Education level: |
Bachelor |
Will Relocate: |
Yes |
Work Experiences
5/2001 - 12/2008
GlaxoSmithKline
Individual Contributor
- Managmen of outsourced preclinical toxicology studies to preferred CROs
1/1998 - 5/2001
GlaxoWellcome
Individual Contributor
- erved as Study Monitor for Safety Pharmacology and Occupational Toxicology studies as well as other nonclinical toxicity studies conducted at contract laboratories
10/1995 - 1/1998
GlaxoWellcome
Manager
- Supervised day-to-day operations of 6 technical staff members
4/1991 - 10/1995
Burroughs Wellcome
Individual Contributor
- Responsible for setting up and executing all assigned study protocols, acute protocol preps, and equipment. Responsible for animal orders, ordering drugs and scheduling of assigned studies
Education
1986
Bachelor Degree
Upper Iowa University
- Biology
1983
Associate Degree
North Iowa Area Community College
- Pre-Physical Therapy