Takeda
Associate Director, Global Regulatory Affairs, Advertising and Pr...
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Overview
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Overview
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).
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