Basic Qualifications:
- Strong understanding of biosimilar regulatory and clinical requirements
- Global biopharmaceutical industry experience
- Experience interacting with policy maker... Jan-11-2012
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5-8 years of experience in regulatory affairs. Qualifed candidates must have been involved in the writing of submissions to the FDA. You must have a Masters degreee at a minimum, preferably in a sc... Jan-26-2012
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