Pharmaceutical Clinical Associates, LLC
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Raritan,
NJ
ESSENTIAL DUTIES AND RESPONSIBILITIES:
1. Assist in the preparation and review of documentation for assigned projects
2. Provide regulatory guidance for specific project work
3. Research, define and communicate global regulatory requirements
4. Ensure regulatory submissions are complete, consistent, and in accordance with FDA/ICH guidelines
5. Liaise with functional representatives to ensure integration of regulatory requirements in development work to provide appropriate documentation for filings
6. Great commitment to excellence, possess both determination and attention to detail, have the ability to produce work to a very high standard
7. Participate in Regulatory Subteam
Experience and Skills:
Contact Dan Meyer at 704.399.4666 or by email dmeyer1@bellsouth.net
Additional Information:
Job Level: Management
Number of Openings: 1
Years of Experience: At least 5 Years
Level of Education: BA/BS
Salary: TBD
Starting Date : March 1, 2010
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Pharmaceutical Clinical Associates is always accepting employment inquiries from professionals interested in our opportunites. If you are interested in career opportunities at Pharmaceutical Clinical Associates please use our online resume formto apply. Pharmaceutical Clinical Associates is an Equal Opportunity Employer.
Raritan, NJ
Raritan, New Jersey
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