Associate Director, Regulatory Affairs Advertising & Promotion (Hybrid)

Associate Director, Regulatory Affairs US Advertising and Promotion
The Associate Director, Regulatory Affairs US Advertising and Promotion is responsible for setting strategy and leading cross‑functional, multidisciplinary therapeutic teams, executing multidivisional initiatives, and leveraging broad industry knowledge to support the company’s mission.

Responsibilities

Make decisions and plans for operations (workflow, assignments, staff development) within area of responsibility with minimal direction.

Set strategy and lead cross‑functional/multidisciplinary therapeutic teams and multidivisional initiatives.

Maintain and evaluate productivity metrics to project current and future business needs.

Align and maintain effective communication channels with key Medical, Marketing, Regulatory, Legal and Public Affairs counterparts; identify areas of improvement in process and policy, develop recommendations and plans, and lead initiatives.

Assist in departmental budget management, identify and communicate budgetary needs to Operations and Finance, and project current and future expenditures and business needs.

Operate independently and consult senior when necessary; if Director absent, assume responsibility for day‑to‑day operations and departmental initiatives with significant impact.

Encourage innovation and hold employees accountable for delivering on goals; mentor, reward, and recommend promotions based on performance.

Exhibit a solid understanding of regulations, guidance from regulatory authorities, political and legal climate, and industry practices related to advertising and promotions to help meet organizational goals.

Develop, implement complex processes and projects, and deliver strategic presentations to senior management.

Minimum Qualifications

Bachelor’s degree.

8+ years of relevant experience (e.g., pharmaceutical, medical device, biologics, pharmacy rotations, public health) OR 6+ years with an advanced degree.

Experience in US Regulatory Affairs Advertising and Promotion.

Experience developing and implementing successful global regulatory strategies.

Preferred Qualifications

Advanced degree preferred: MS, MPH, MSN, PA, DNP, PhD, PharmD, JD, MD.

Experience in a management capacity.

Other Required Skills

Experience working in a complex and matrix environment.

Strong communication skills, both oral and written.

Benefits & Compensation

Base pay compensation range: the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting, based on the job grade for this position; actual compensation depends on geographic location and other factors and may be modified in the future.

Comprehensive benefits package: paid time off (vacation, holidays, sick), medical, dental, vision insurance, and 401(k) for eligible employees.

Short‑term incentive programs.

Eligibility for bonus, commission, incentive, and other compensation and benefits remains at the Company’s sole and absolute discretion, consistent with applicable law.

AbbVie is an equal‑opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only – to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

#J-18808-Ljbffr