Manage programs/products as internal expert on US and international codes, guidance, and industry standards related to prescription medicine promotion. Serve as Subject Matter Expert for assigned products and projects focusing on advertising and promotion regulatory affairs. Provide regulatory guidance during development, review, approval, and implementation of medical and commercial materials. Lead the global Medical, Legal, and Regulatory review process (CMRP). • Subject Matter Expert for assigned products and projects focusing on advertising and promotion regulatory affairs.
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