Associate Director, Global Regulatory Affairs, Advertising and Promotion

Join Takeda as an Associate Director, Global Regulatory Affairs, Advertising and Promotion.

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).