Associate Director, Regulatory Affairs — Ad Promo Strategy

Teva Pharmaceuticals; West Chester (Chester County); On-site; USD 140,000 - 175,000; Full time

Benefits offered by this job

Career development platform

Flexible working schedules

Comprehensive benefits package

Job summary

Teva Pharmaceuticals seeks an Associate Director of Regulatory Affairs (Advertising and Promotion) to lead regulatory review and approval of promotional materials across channels. You will chair PARC reviews, ensure substantiation, and collaborate with Medical, Legal, Commercial teams to maintain truthful, non-misleading communications.

The role reports to the Senior Director and supports multiple product portfolios, driving strategy for launch materials and 2253 submissions while tracking OPDP

Qualifications

• Bachelor's degree in life sciences, pharmacy, or related field preferred; advanced degree a plus.
• 4 years of pharmaceutical or biotechnology regulatory affairs experience; 2+ years in Advertising and Promotion review.

Responsibilities

• Lead regulatory review and approval of promotional materials across channels (HCP, DTC, digital, social).
• Chair PARC reviews and ensure claims substantiation, fair balance and compliance with labeling.
• Collaborate with Legal, Medical, and Commercial teams on promotional practice and enforcement trends.
• Oversee 2253 submissions and serve as regulatory contact for OPDP correspondence.

Skills

Regulatory affairs knowledge

Analytical judgment

Communication skills

Cross-functional collaboration

Project management

Education

Bachelor's degree in life sciences

PharmD, MS, or PhD (advanced degree)

Tools

Veeva Vault PromoMats

Zinc MAPS

Job description

Teva Pharmaceuticals seeks an Associate Director of Regulatory Affairs (Advertising and Promotion) to lead regulatory review and approval of promotional materials across channels. You will chair PARC reviews, ensure substantiation, and collaborate with Medical, Legal, Commercial teams to maintain truthful, non-misleading communications.

The role reports to the Senior Director and supports multiple product portfolios, driving strategy for launch materials and 2253 submissions while tracking OPDP