• Act as a Subject Matter Expert for assigned products and projects focusing on advertising and promotion regulatory affairs. • Provide regulatory guidance throughout development, review, approval, and implementation of medical and commercial materials. • Lead the global Medical, Legal, and Regulatory review process (CMRP). Maintain compliance with EFPIA, IFPMA, FDA codes, and regulations. The ideal candidate should possess 8+ years of pharmaceutical industry experience, including regulatory expertise, knowledge of international advertising and promotion standards, and change management and problem-solving skills.
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