Associate Director, Global Regulatory Affairs, Advertising and Promotion

Overview

The following information aims to provide potential candidates with a better understanding of the requirements for this role.

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.

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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