Associate Director, Global Regulatory Affairs, Advertising and Promotion

Takeda; Seattle (WA); Remote; USD 153,000 - 242,000; Full time

Job summary

A global pharmaceutical company is seeking an Associate Director for Global Regulatory Affairs, Advertising and Promotion. The role requires managing regulatory programs and ensuring compliance with industry standards. Strong communication, negotiation, and leadership skills are essential, along with 8+ years of experience in the pharmaceutical sector. The position offers a competitive salary range and is based in Seattle, WA with potential for remote work.

Qualifications

• 8+ years of pharmaceutical industry experience, including regulatory experience.
• Knowledge of international advertising and promotion standards.

Responsibilities

• Serve as Subject Matter Expert for assigned products and projects.
• Provide regulatory guidance during development, review, approval, and implementation.
• Lead the global Medical, Legal, and Regulatory review process.
• Act as a strategic partner throughout the product lifecycle.
• Ensure compliance with EFPIA, IFPMA, FDA codes, and regulations.

Skills

Strong communication

Negotiation skills

Leadership

Strategic thinking

Change management

Problem-solving skills

Interpersonal skills

Presentation skills

Education

BSc Degree or BA

Job description

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.

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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