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Associate Director Regulatory Affairs Job
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| Employer Name: PharmaceuticalCrossing |
SpiderID: 2397929 |
| Location: La Jolla, California |
Date Posted: 7/26/2008 |
| Wage: |
Category: Medical/Health |
| Job Code: 6847891 |
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Job Description:
This position interfaces with experimental medicine, preclinical, discovery research, chemistry, clinical research, clinical operations, and project management. This interface occurs at the early development compound development team meetings and at subteam meetings. The early development compound development team is responsible for developing the compound from first in man to proof of concept. Qualifications A minimum of a Bachelors degree in relevant life or health-related science is required. A minimum of 6 years related industry (pharmaceutical) experience in regulatory affairs is also required. Some of this experience should be with US IND filings (experience with CTAs in addition is also helpful). Previous experience with early development activities (e.g., nonclinical studies, pre- planning) for small molecules is preferred. Previous experience with electronic submissions is preferred. Proficient in the use of technology including MS Office Software Packages and Internet, for word-processing, spreadsheet analysis, database analysis, Internet research, etc. Experience in using MS Word and Adobe Acrobat for submission creation is preferred.
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Job Criteria:
Start Date:
Position Type: Full-Time Permanent
Years of Experience Required:
Education Required:
Overnight Travel:
Vacation Time:
Contact Information:
| Contact Name: - |
Company Type: Employer |
| Company: PharmaceuticalCrossing |
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| City: Pasadena |
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| State: California |
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| Zip: |
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Web Site: http://www.pharmaceuticalcrossing.com
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