Takeda
Associate Director, Global Regulatory Affairs, Advertising and Promotion
Takeda, Seattle, Washington, us, 98127
Associate Director, Global Regulatory Affairs, Advertising and Promotion Join Takeda as an
Associate Director, Global Regulatory Affairs, Advertising and Promotion .
Is this the next step in your career Find out if you are the right candidate by reading through the complete overview below. This role involves managing programs/products as the internal expert on US and international codes, guidance, and industry standards related to prescription medicine promotion. Key Responsibilities:
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). Act as a strategic partner throughout the product lifecycle, from clinical development to marketing maintenance. Ensure compliance with EFPIA, IFPMA, FDA codes, and regulations. Minimum Qualifications:
BSc Degree (preferred) or BA. 8+ years of pharmaceutical industry experience, including regulatory experience. Knowledge of international advertising and promotion standards. Strong communication, negotiation, and leadership skills. Additional Skills:
Leadership and strategic thinking. Change management and problem-solving skills. Excellent interpersonal and presentation skills. About Takeda: Takeda is committed to transforming patient care through innovation, fostering an inclusive and collaborative workplace, and delivering better health worldwide. Compensation & Benefits: Base salary range: $153,600 - $241,340 per year, with additional incentives and benefits. Location: Massachusetts (Remote).
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Associate Director, Global Regulatory Affairs, Advertising and Promotion .
Is this the next step in your career Find out if you are the right candidate by reading through the complete overview below. This role involves managing programs/products as the internal expert on US and international codes, guidance, and industry standards related to prescription medicine promotion. Key Responsibilities:
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). Act as a strategic partner throughout the product lifecycle, from clinical development to marketing maintenance. Ensure compliance with EFPIA, IFPMA, FDA codes, and regulations. Minimum Qualifications:
BSc Degree (preferred) or BA. 8+ years of pharmaceutical industry experience, including regulatory experience. Knowledge of international advertising and promotion standards. Strong communication, negotiation, and leadership skills. Additional Skills:
Leadership and strategic thinking. Change management and problem-solving skills. Excellent interpersonal and presentation skills. About Takeda: Takeda is committed to transforming patient care through innovation, fostering an inclusive and collaborative workplace, and delivering better health worldwide. Compensation & Benefits: Base salary range: $153,600 - $241,340 per year, with additional incentives and benefits. Location: Massachusetts (Remote).
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