Associate Director, Regulatory Affairs Advertising and Promotion

Job Description Summary #LI-Hybrid As the Associate Director, Regulatory Affairs Advertising & Promotion you will provide strategic regulatory advice on advertising/promotion and medical materials to the US organization for assigned products in accordance with business goals and objectives, FDA regulations/guidances, PhRMA guidelines, and company policy. This position will be located at the East Hanover site and will not have the ability to be located remotely. This position will require 20% travel as defined by the business (domestic and/or international). Please note that this role would not provide relocation, and only local candidates will be considered. Job Description Responsibilities Serves as a primary regulatory advertising and promotion reviewer for assigned products on Materials Approval Process ("MAP") teams. May include a launch product or indication with manager oversight. Liaison with OPDP regarding advertising and promotion for assigned products, including products approved under Subpart H with manager oversight. Establishes strong and positive working relationship with OPDP reviewers. Manages OPDP queries on assigned products. Applies regulatory and therapeutic area knowledge to Brand Team's objectives and initiatives to develop solutions to US promotional issues. Ensures regulatory compliance while effectively managing business risks. Maintains awareness of competitive activities by monitoring major US Medical meetings where assigned therapeutic area products are promoted. Prepares complaint letters to OPDP with manager oversight. Conduct reviews of materials to be used by medical personnel in discussions with customers. Monitors US regulatory promotional environment by reviewing regulatory promotional guidelines, untitled and warning letters to pharmaceutical companies published by OPDP, and by attendance of major FDLI, DIA and other industry/FDA meetings. Collaborates with Regulatory Affairs colleagues to provide input to study designs or US label regarding feasibility of promoting potential data/claims with manager oversight. Participates/assists in US labeling negotiations and FDA meetings as necessary. Ensures that changes in US Prescribing Information are reflected in current promotion and advertising. Essential Requirements BS Degree or equivalent. Advanced degree desirable (MS, PhD, PharmD, or JD) Minimum 2 years regulatory experience or related medical information and/or promotional review experience. Knowledge and understanding of US regulations for drug promotion/advertising and US labeling Understanding of business goals of the involved business franchise, marketing concepts and tools Must be able to work in a multi-disciplinary environment Must process strong interpersonal and communication skills Must have analytical and problem‑solving skills associated with problem review and inquiries. Must be able to provide creative solutions to problems Desirable Requirements Ability to analyze and interpret efficacy and safety data desired Compensation Summary The salary for this position is expected to range between $145,600 and $270,400 per year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance‑based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US‑based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous Salary Range: $145,600.00 - $270,400.00 EEO Statement The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. Accessibility and reasonable accommodations The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e‑mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Skills Desired Clinical Trials Cross‑Functional Teams Detail‑Oriented Drug Development Lifesciences Negotiation Skills Problem Solving Skills Regulatory Compliance Risk Management #J-18808-Ljbffr