Key Accountabilities: • Function as Subject Matter Expert for assigned products and projects focusing on advertising and promotion regulatory affairs. • Offer authoritative guidance during development, review, approval, and implementation of medical and commercial materials. • Direct the global Medical, Legal, and Regulatory review process (CMRP). • Ensure compliance with EFPIA, IFPMA, FDA codes, and regulations. Essential Qualifications: • 8+ years of pharmaceutical industry experience, including regulatory experience.
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