The position requires a professional with expertise in managing programs/products as the internal subject matter expert on US and international codes, guidance, and industry standards related to prescription medicine promotion. • Offer regulatory guidance during development, review, approval, and implementation of medical and commercial materials. • Oversee the global Medical, Legal, and Regulatory review process (CMRP). • Maintain compliance with EFPIA, IFPMA, FDA codes, and regulations. Qualifications: A minimum of 8 years of experience in the pharmaceutical industry, including regulatory experience, is required.
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